FDA 510(k) Applications Submitted by MERIDIAN MEDICAL TECHNOLOGIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030104 | 01/13/2003 | PRIME ECG SYSTEM | MERIDIAN MEDICAL TECHNOLOGIES, INC. |
| K012414 | 07/30/2001 | PRIME ECG SYSTEM | MERIDIAN MEDICAL TECHNOLOGIES, INC. |
| K965101 | 12/20/1996 | CARDIOBEEPER CB-12L | MERIDIAN MEDICAL TECHNOLOGIES, INC. |
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