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Braemar Corp.

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

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K030856	ER800 SERIES ECG EVENT RECORDER	MWJ	2003-03-28	View
510(k)	K993617	DIGITRAKPLUS HOLTER RECORDER	MWJ	1999-11-24	View
510(k)	K993618	DXP1000 HOLTER RECORDER	MWJ	1999-11-24	View
510(k)	K981394	BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720	DXH	1998-09-28	View
510(k)	K945130	BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER	DSH	1995-04-12	View

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