ONQ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Electrosurgical Coagulation For Aesthetic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Medical specialty
- General, Plastic Surgery
- Flags
- Third-party review eligible
- FDA definition
- For the treatment of spider vein or telangiectasia by thermocoagulation.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MED RF 4000 (K210077) | F Care Systems USA, LLC | 2021-12-17 |
| EVRF SYSTEM (K130283) | F Care Systems NV | 2013-03-07 |
| VEIN-GOGH INSTRUMENT (K112334) | Refine USA, LLC | 2012-05-08 |
| VEINWAVE, TC3000 (K083352) | Newlands Clinical Trials, Ltd. | 2009-06-12 |
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Every clearance here is in the API, with alerts when new ones post.