FDA Product Code
FDA Product Code KOQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Dental
- 21 CFR Citation
- 872.3410
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K901882 | URESIL ENDOSCOPIC LASER OVERTUBE | Uresil Corp. | 1990-07-27 | Traditional | PDF ↗ |
| K896821 | OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE | North American Sterilization & Packaging Co. | 1990-02-09 | Traditional | PDF ↗ |
| K900401 | NAS&P GRASPING FORCEPS & ASSOC. DEVICES | North American Sterilization & Packaging Co. | 1990-02-09 | Traditional | PDF ↗ |
| K831265 | DENTOLOCK DENTURE ADHESIVE CREAM | Solar Dental Co., Inc. | 1983-05-09 | Traditional | PDF ↗ |
Product code KOQ · Class I · Dental. Data: openFDA.