Daesung Maref Co., Ltd.
FDA 510(k) & PMA Approved Devices — 13 products
Advertisement
Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231437 | LF900 | IRP | 2023-07-19 | View |
| 510(k) | K202395 | SP-1000, SP-2000 | IRP | 2021-09-01 | View |
| 510(k) | K203498 | LX9max | IRP | 2021-07-02 | View |
| 510(k) | K203019 | LF900 | IRP | 2021-06-22 | View |
| 510(k) | K203353 | DVT-PRO | JOW | 2021-04-22 | View |
| 510(k) | K203417 | DVT-4000S | JOW | 2021-03-28 | View |
| 510(k) | K203016 | DVT-2600 | JOW | 2020-12-05 | View |
| 510(k) | K160178 | Lympha-Flow(LF1200) | IRP | 2017-01-11 | View |
| 510(k) | K160180 | Intermittent Pneumatic Compression system | JOW | 2016-11-03 | View |
| 510(k) | K150980 | Venous Assist System | JOW | 2016-05-12 | View |
| 510(k) | K112441 | COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM | IRP | 2012-01-17 | View |
| 510(k) | K112677 | THE VENOUS ASSIST SYSTEM | JOW | 2012-01-13 | View |
| 510(k) | K102320 | COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL LX7(V7) | IRP | 2011-03-04 | View |
No matching devices.
Advertisement