FDA Product Code
FDA Product Code FYI — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.3250
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K871073 | OMEGA BIVALVE NASAL SPLINTS | Omega Silicone, Inc. | 1987-05-11 | Traditional | PDF ↗ |
| K821178 | ETHICON EXTERNAL FIXATION WIRE | ETHICON, Inc. | 1983-06-11 | Traditional | PDF ↗ |
| K801072 | STRAITH NASAL SPLINT | Surgical Technology Laboratories, Inc. | 1980-06-17 | Traditional | PDF ↗ |
| K792106 | CONPHAR O.R. HEAD COVER-STERILE | Conphar, Inc. | 1979-11-05 | Traditional | PDF ↗ |
Product code FYI · Class I · General, Plastic Surgery. Data: openFDA.