FDA 510(k) Applications Submitted by BRAEMAR CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030856 | 03/18/2003 | ER800 SERIES ECG EVENT RECORDER | BRAEMAR CORP. |
| K981394 | 04/17/1998 | BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720 | BRAEMAR CORP. |
| K993617 | 10/26/1999 | DIGITRAKPLUS HOLTER RECORDER | BRAEMAR CORP. |
| K993618 | 10/26/1999 | DXP1000 HOLTER RECORDER | BRAEMAR CORP. |
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