Meridian AG
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2024-01-25
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232417 | MR Q; MR Q SUPINE; MR Q SLT | HQF | 2024-01-25 | View |
| 510(k) | K231011 | Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse | HQF | 2023-09-12 | View |
| 510(k) | K160677 | MICRORUPTOR 6 | GEX | 2017-05-19 | View |
No matching devices.