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Oakfield Instruments, Ltd.

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

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K964804	FLEXILOG LS	KLA	1997-08-06	View
510(k)	K964589	FLEXILOG 3000	KLA	1997-03-04	View
510(k)	K961895	FLEXILOG LS 13921	KLA	1996-11-04	View
510(k)	K945069	FLEXILOG 2000	FFT	1995-06-13	View
510(k)	K920115	MEDISCINT	IZD	1992-03-30	View
510(k)	K902460	CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)	IZD	1990-08-28	View
510(k)	K896288	FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM	FFT	1990-05-04	View
510(k)	K894902	SOURCERER	JJJ	1989-10-17	View

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