KCQ — Tube Impression And Matrix Class I
FDA product code KCQ covers "Tube Impression And Matrix", a Class I medical device regulated under 21 CFR 872.6570. Submissions are reviewed by the Dental panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KCQ
- Device Class
- Class I
- Regulation Number
- 872.6570
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K896621 | intl. medical marketing | L.T.C. REPLACEMENT GASTROSTOMY TUBE | March 13, 1990 |