Qmed, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972991 | MONITOR ONE NDX | DPS | 1998-12-03 | View |
| 510(k) | K932109 | PROFILOMAT | DXN | 1993-12-03 | View |
| 510(k) | K921476 | INTERP-1000 | LOS | 1992-10-21 | View |
| 510(k) | K897121 | QEKG ELECTROCARDIOGRAPH | DPS | 1990-04-30 | View |
| 510(k) | K873591 | A.R.M. (ASPEN RETURN MONITOR) | GEI | 1987-09-30 | View |
| 510(k) | K862377 | QMED SELF ADHERING ELECTRODE | GXY | 1986-09-26 | View |
| 510(k) | K863091 | BICORD BY QMED | HAM | 1986-08-29 | View |
| 510(k) | K861437 | QMED SYSTEM 2150 | DXG | 1986-05-20 | View |
| 510(k) | K843559 | KLEENIT BY QMED | 1984-10-24 | View | |
| 510(k) | K841172 | MONITOR ONE | DSI | 1984-07-27 | View |
| 510(k) | K840465 | Q-MED ELECTRODE | DRX | 1984-06-19 | View |
No matching devices.
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