KOQ — Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&) Class I
FDA Device Classification
Classification Details
- Product Code
- KOQ
- Device Class
- Class I
- Regulation Number
- 872.3410
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K901882 | uresil | URESIL ENDOSCOPIC LASER OVERTUBE | July 27, 1990 |
| K896821 | north american sterilization and packaging | OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE | February 9, 1990 |
| K900401 | north american sterilization and packaging | NAS&P GRASPING FORCEPS & ASSOC. DEVICES | February 9, 1990 |
| K831265 | solar dental co | DENTOLOCK DENTURE ADHESIVE CREAM | May 9, 1983 |