Braemar Corp.

5 FDA 510(k) medical device clearances.

Top product codes for Braemar Corp.

Recent clearances by Braemar Corp.

K030856 — ER800 SERIES ECG EVENT RECORDER MWJ · 2003-03-28
K993617 — DIGITRAKPLUS HOLTER RECORDER MWJ · 1999-11-24
K993618 — DXP1000 HOLTER RECORDER MWJ · 1999-11-24
K981394 — BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720 DXH · 1998-09-28
K945130 — BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER DSH · 1995-04-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.