Watermark Medical
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) | K160499 | Apnea Risk Evaluation System (ARES), Model 620 | MNR | 2017-04-24 | View |
| 510(k) | K120325 | CONNECTED CARE MOBILE APPLICATION | DRG | 2012-07-18 | View |
| 510(k) | K120470 | MIPAL | DRG | 2012-06-08 | View |
No matching devices.
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