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Cardio Kinetics, Inc.

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

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K823215	CKG 8800	DSB	1982-11-24	View
510(k)	K822020	CKG 8000	DSB	1982-08-06	View
510(k)	K801485	SERIES 602 CKG RECORDER (MODIFIED)	DSF	1980-07-08	View
510(k)	K800851	SERIES 602 CKGTM RECORDER	DSF	1980-04-24	View
510(k)	K792051	CKG CARDIOKYMOGRAPH	DSB	1979-11-13	View

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