Meridian Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K030104 | PRIME ECG SYSTEM | DPS | 2003-06-11 | View |
| 510(k) | K012414 | PRIME ECG SYSTEM | DPS | 2002-03-06 | View |
| 510(k) | K965101 | CARDIOBEEPER CB-12L | DXH | 1997-03-17 | View |
No matching devices.
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