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

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K954596	PRO-B CORE-RECT COAXIAL BIOPSY SYSTEM	FCG	1995-10-07	View
510(k)	K952350	JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)	LWE	1995-07-17	View
510(k)	K951598	PRO-B BIOPSY NEEDLE	FCG	1995-04-21	View
510(k)	K944944	CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE	FCG	1994-12-21	View
510(k)	K944942	BREAST LESION LOCALIZATION NEEDLE	GDF	1994-11-04	View

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