Dynatech/Nevada, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Advertisement
Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K942546 | CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZER | DXN | 1995-01-27 | View |
| 510(k) | K935817 | MEDSIM 300 PATIENT SIMULATOR | DRT | 1994-01-18 | View |
| 510(k) | K934254 | IMPULSE 3000 DEFIBRILLATOR ANALYZER | DRL | 1993-11-23 | View |
| 510(k) | K897074 | MODEL 215M PATIENT SIMULATOR | DSI | 1990-05-17 | View |
| 510(k) | K897029 | MODEL ECG100 SIMULATOR | DPS | 1990-04-26 | View |
| 510(k) | K897096 | MODEL 404A I.V. INFUSION PUMP ANALYZER | FRN | 1990-03-15 | View |
No matching devices.
Advertisement