FDA 510(k) Applications Submitted by GERARD LYNN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K002310 | 07/31/2000 | CARDIOBEEPER CB12/12, MODEL CB12/12 | MERIDIAN MEDICAL TECHNOLOGIES LTD. |
| K983582 | 10/13/1998 | CARDIOBEEPER CB250 | MERDIAN MEDICAL TECHNOLOGIES LTD. |
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