FDA 510(k) Applications Submitted by RAYMOND COHEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970298 | 01/27/1997 | DM-400 HOLTER ECG CASSETTE RECORDER | DIAGNOSTIC MONITORING |
| K970741 | 02/28/1997 | POWERHEART AECD | CARDIAC SCIENCE, INC. |
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