FDA Product Code
FDA Product Code QUQ — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4400
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K220891 | Kahook Dual Blade Glide (KDB Glide) | New World Medical, Inc. | 2024-05-17 | Traditional | PDF ↗ |
Product code QUQ · Class II · General, Plastic Surgery. Data: openFDA.