Automated Screening Devices
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) | K792653 | SENTRY | DXN | 1980-01-04 | View |
| 510(k) | K782000 | MONITOR, NON-INVASIVE BLOOD PRESSURE | DXN | 1978-12-05 | View |
No matching devices.
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