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Diagnostic Monitoring Software

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K062959	DMS 300-2, 300-3 AND 300-4	MWJ	2006-10-16	View
510(k)	K062088	PREMIER 11 HOLTER	MLO	2006-08-25	View
510(k)	K062007	DMS 300-7	DSH	2006-08-16	View
510(k)	K911615	HOLTER 24-HOUR ECG SYSTEM, MODEL NUMBER: DMS 300	DQK	1992-01-08	View

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