FDA Product Code
FDA Product Code MUK — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4400
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K020952 | SURX RF SYSTEM | Surx, Inc. | 2002-05-30 | Traditional | PDF ↗ |
| K020126 | MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM) | Surx, Inc. | 2002-03-15 | Traditional | PDF ↗ |
| K011190 | SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM) | Surx, Inc. | 2002-01-08 | Traditional | PDF ↗ |
Product code MUK · Class II · General, Plastic Surgery. Data: openFDA.