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Progene Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K895294	PROGENE IGE BEAD EIA	DGC	1989-09-21	View
510(k)	K882538	PROGENE MICROALBUMINURIA SCREEN	JIR	1989-03-13	View
510(k)	K875125	PROGENE(TM) IGE TEST	DHB	1988-02-25	View

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