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Proact, Ltd.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K941256	QUICK CORE II	KNW	1994-07-13	View
510(k)	K926559	PROACT BIOPSY NEEDLE ENCHANCEMENTS	FCG	1993-03-22	View
510(k)	K913306	BONE-TEMNO/STERNUM-TEMNO	LWE	1991-11-01	View
510(k)	K902320	BAUER FLEXI-TEMNO BIOPSY NEEDLE	FCG	1990-10-01	View
510(k)	K902319	BAUER TEMNO BIOPSY NEEDLE	FCG	1990-09-06	View

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