BIOCONTROL TECHNOLOGY INC
8-K, 1997-07-23
ELECTROMEDICAL & ELECTROTHERAPEUTIC APPARATUS
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               SECURITIES AND EXCHANGE COMMISSION
                                
                     Washington, D.C.  20549
                                
                                
                            FORM 8-K
                                
                                
                         CURRENT REPORT
                                
             Pursuant to Section 13 or 15(d) of the
                 Securities Exchange Act of 1934

                       ___________________


 Date of Report (Date of earliest event reported) July 23, 1997

                   BIOCONTROL TECHNOLOGY, INC.
     (Exact name of registrant as specified in its charter)


         Pennsylvania                0-10822               25-1229323
(State of other jurisdiction (Commission File Number)    (IRS Employer
       of incorporation)                              Identification No.)


      300 Indian Springs Road, Indiana, Pennsylvania 15701
    (Address of principal executive offices)       (Zip Code)


Registrant's telephone number, including area code (412) 349-1811
                                
                                
                                
_________________________________________________________________
                 (Former name or former address,
                  if changes since last report.)
                                
                                
                                
                                
Item 1.   Change in Control of Registrant.
          Not applicable.

Item 2.   Acquisition or Disposition of Assets.
          Not applicable.

Item 3.   Bankruptcy or Receivership.
          Not applicable.

Item 4.   Changes in Registrant's Certifying Accountant
          Not applicable.

Item 5.   Other Events.
            On   July  18,  1997,  Biocontrol  Technology,   Inc.
(NASDAQ:BICO) announced that a  510(k)  Notification has been
submitted to the Food  and  Drug Administration  (FDA)  by
HemoCleanse,  Inc.,  which  works   in conjunction with BICO
subsidiary, IDT, Inc.  The 510(k)  requests market  clearance for
the ThermoChem HT System (ThermoChem)  for use  in  Intraperitoneal
Hyperthermic Chemotherapy  (IPHC).  The ThermoChem  HT System was
formerly known as the BioLogic-HTA,  a part  of the BioLogic-HT
System, currently being tested by  IDT, Inc.,  in  conjunction
with HemoCleanse,  Inc.,  for  whole-body extracorporeal hyperthermia
treatment of cancer and HIV/AIDS.

Item 6.   Resignation of Registrant's Directors.
          Not Applicable

Item 7.   Financial Statement, Pro Forma Financial Information
          and Exhibits.

          (a)  Financial Statements and Businesses Acquired - Not
               Applicable.

          (b)  Pro Forma Financial Information - Not Applicable.

          (c)  Exhibits-Press Release

                           SIGNATURES

      Pursuant to the requirement of the Securities Exchange  Act
of  1934, the Registrant has duly caused this Report to be signed
on its behalf by the undersigned hereunto duly authorized.

                                   BIOCONTROL TECHNOLOGY, INC.


                                   by  /s/  Fred E. Cooper
                                            Fred E. Cooper, CEO

DATED:  July 23, 1997


                                       BIOCONTROL TECHNOLOGY, INC
                            2275 Swallow Hill Road, Building 2500
                                            Pittsburgh, PA  15220
Press Release

Release:  Immediate

For More Information, Call:

Investors                                          Media
Diane McQuaide
Susan Taylor
1.412.429.0673  phone
1.412.279.9455 phone
1.412.279.9690  fax
1.412.279.9447 fax


 510(K) SUBMITTED TO FDA ON PRODUCT TO BE MARKETED BY BIOCONTROL
                         SUBSIDIARY, IDT

     Pittsburgh, PA - July 23, 1997 - Biocontrol Technology, Inc.
(Nasdaq:BICO) announced today that a 510(k) Notification has been
submitted   to  the  Food  and  Drug  Administration   (FDA)   by
HemoCleanse,   Inc.,  which  works  in  conjunction   with   BICO
subsidiary,  IDT, Inc.  The 510(k) requests market clearance  for
the ThermoChem HT System (ThermoChem) for use in Intraperitoneal
Hyperthermic Chemotherapy (IPHC).
      HemoCleanse, Inc., of West Lafayette, IN, manufactures  the
ThermoChem  while IDT holds exclusive worldwide marketing  rights
to the ThermoChem and related disposables.
     The ThermoChem HT System was formerly known as the BioLogic-
HTA,  a part of the BioLogic-HT System, currently being  tested
by  IDT, Inc., in conjunction with HemoCleanse, Inc., for  whole-
body   extracorporeal  hyperthermia  treatment  of   cancer   and
HIV/AIDS.  The product name was changed to provide clear  product
identification in the intended market.
      The ThermoChem HT System heats and/or cools fluids, such as
chemotherapy  agents in solution, and recirculates  these  fluids
into   the  peritoneal  (abdominal)  cavity,  thus  providing   a
hyperthermic condition for combined cancer therapy.
      ThermoChem and related disposables are intended to be  used
in  a  hospital  operating  room and in ambulatory  settings  for
patients  with  gastrointestinal and  other  cancers  within  the
peritoneal cavity.
           Biocontrol Technology, Inc. has its corporate  offices
in  Pittsburgh,  PA  and  is  involved  in  the  development  and
manufacture  of  biomedical devices and  environmental  products.
IDT,  Inc., a wholly-owned subsidiary of Biocontrol also  located
in  Pittsburgh, PA, holds exclusive worldwide marketing rights to
the ThermoChem HT System, which is manufactured by HemoCleanse




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