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Clinical Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K971653	GLUCOCHEK POCKETLAB II BLOOD GLUCOSE SYSTEM	CGA	1998-01-02	View
510(k)	K951457	GLUCOCHEK POCKETLAB	CGA	1996-02-22	View
510(k)	K940215	GLUCOCHEK	CGA	1995-01-17	View
510(k)	K854903	GORDON DIAGNOSTIC SYSTEM MODEL I	LQD	1986-06-02	View
510(k)	K771813	CENTRIFICHEM SYS 400 ANALYZER	JJG	1977-10-25	View
510(k)	K771118	CENTRIA SEPARATION COLUMNS TYPE A	CEM	1977-07-11	View
510(k)	K771117	CENTRIA CORTISOL RIA	CGR	1977-06-23	View
510(k)	K761272	CENTRIA T4 RIA	CDX	1977-03-16	View

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