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FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K953676 | BREEZE DIGITAL INFLATION DEVICE | MAV | 1996-03-29 | View |
| 510(k) | K951722 | PERCEPTOR COMPENSATOR MORSE MANIFOLD | DRS | 1996-03-25 | View |
| 510(k) | K921322 | MORSE ANESTHESIA MANIFOLD | FPA | 1993-07-09 | View |
| 510(k) | K822100 | HIGH PRESSURE CONTRAST INJECTION LINE | DQO | 1982-08-24 | View |
| 510(k) | K813549 | CONTINUOUS FLUSH DEVICE | DRS | 1982-01-12 | View |
| 510(k) | K790082 | ARTERIAL EXTENSION SET | DQO | 1979-01-25 | View |
| 510(k) | K790083 | CATHETER, ARTERIAL LINE | DQY | 1979-01-25 | View |
| 510(k) | K782095 | STOPCOCKS, MANIFOLDS | DTL | 1979-01-23 | View |
No matching devices.
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