FDA Product Code
FDA Product Code FQP — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4580
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K001223 | ACULUX, MODEL AX3001, AX3002 | Aculux | 2000-06-23 | Traditional | PDF ↗ |
| K993314 | SYNTHES LIGHT GUIDE | Synthes (Usa) | 1999-12-06 | Abbreviated | PDF ↗ |
| K781581 | SURGICAL LIGHT 22 SERIES | American Sterilizer Co. | 1978-10-17 | Traditional | PDF ↗ |
| K770812 | HANDLES, LIGHT, SURGICAL, STEOILE | Sybron Corp. | 1977-05-23 | Traditional | PDF ↗ |
| K761018 | SURGICAL LIGHT - CHALLENGE 22 SERIES | Amsco Co. | 1977-01-26 | Traditional | PDF ↗ |
Product code FQP · Class II · General, Plastic Surgery. Data: openFDA.