FDA Product Code
FDA Product Code ONQ — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4400
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K210077 | MED RF 4000 | F Care Systems USA, LLC | 2021-12-17 | Traditional | PDF ↗ |
| K130283 | EVRF SYSTEM | F Care Systems NV | 2013-03-07 | Traditional | PDF ↗ |
| K112334 | VEIN-GOGH INSTRUMENT | Refine USA, LLC | 2012-05-08 | Traditional | PDF ↗ |
| K083352 | VEINWAVE, TC3000 | Newlands Clinical Trials, Ltd. | 2009-06-12 | Traditional | PDF ↗ |
Product code ONQ · Class II · General, Plastic Surgery. Data: openFDA.