FDA Product Code
FDA Product Code KXX — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Dental
- 21 CFR Citation
- 872.3450
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K863375 | SEA-BOND | Combe, Inc. | 1986-09-19 | Traditional | PDF ↗ |
Product code KXX · Class I · Dental. Data: openFDA.