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Dynagen, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K963733	NICCHECK I	MRS	1996-12-13	View
510(k)	K943051	MYCOAKT M. TUBERCULOSIS CUULTURE ID KIT	JSY	1995-03-13	View
510(k)	K943050	MYCOAKT M KANSASII CULTURE ID KIT	JSY	1995-03-13	View
510(k)	K943049	MYCOAKT M. AVIUM CULTURE ID KIT	JSY	1995-03-13	View
510(k)	K931105	PROCHECK(TM) BLIND PERFORMANCE SPECIMENS	DIF	1993-04-21	View
510(k)	K912888	URITEC TEST STRIP & HUMAN URINE + & - TEST CONTROL	MIG	1992-02-24	View

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