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Columbus Instruments Intl. Corp.

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

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K895791	OXYMAX	BZL	1990-03-28	View
510(k)	K861543	CARDIOMAX-II	DXG	1987-03-10	View
510(k)	K861100	ISO-THERMEX	FLL	1986-05-12	View
510(k)	K782036	TREMOR MONITOR	GYD	1979-01-23	View
510(k)	K771718	CARDIOTHERM-500X	DXG	1977-09-28	View

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