EMK — Curette, Surgical, Dental Class I
FDA product code EMK covers "Curette, Surgical, Dental", a Class I medical device regulated under 21 CFR 872.4565. 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
- EMK
- Device Class
- Class I
- Regulation Number
- 872.4565
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K851718 | artiberia | 930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES | July 2, 1985 |