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Cryomedical Sciences, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K011073	CRYOPLAN SYSTEM	GEH	2001-08-22	View
510(k)	K982055	ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880	GEH	1998-09-08	View
510(k)	K980668	CMS BLIZZARD 700 SERIES MODELS 730, 740,750,760,770,780 & 790	GEH	1998-07-17	View
510(k)	K980670	CMS BLIZZARD 700 SERIES MODELS 710, 711, 712, 720, 721 AND 722	GEH	1998-07-17	View
510(k)	K973190	ACCUPROBE 450, ACCUPROBE 550/530 AND THE ACCUPROBE 600 SERIES	GEI	1997-11-21	View
510(k)	K970995	CMS CRYOLITE	GEH	1997-07-07	View
510(k)	K964336	CMS ACCUPROBE 610, 620, 630, 640, 650, 660, 670, 680	GEH	1997-03-20	View
510(k)	K953637	CMS ACCUPROBE 550/530	GEH	1995-12-04	View
510(k)	K952895	CMS URETHRAL WARMER	GEH	1995-10-24	View
510(k)	K904421	CMS ONCOPROBE (TM)	GEH	1991-04-08	View

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