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Press Release


Pittsburgh, PA - November 14, 1996 - Biocontrol Technology, Inc. (NASDAQ:BICO) announced today that its top executives and scientists met with the Food and Drug Administration (FDA) late Wednesday afternoon, November 13, 1996, regarding the Company's recently submitted 510(k) for the Diasensor 1000TM noninvasive glucose sensor for diabetics.

At the meeting, discussion centered around the FDA's request for an in-home study to finalize the approval process.

Biocontrol will therefore respond to the FDA as soon as possible with a proposed in-home study plan.

The Company further announced that its 510(k) has been withdrawn by the FDA since it will need to be amended with the in-home study data.

Biocontrol Technology, Inc. has its corporate offices in Pittsburgh, PA and is involved in the development and manufacture of biomedical devices and environmental products.


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Last Updated: Thursday February 27, 2014 19:28:21
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