Medical Electronics Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K873533 | SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE | DSI | 1988-01-29 | View |
| 510(k) | K872249 | SIRECUST MODEL 960 AND 961 PATIENT MONITORING | DRT | 1987-07-21 | View |
No matching devices.
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