EKE — Curette, Operative Class I
FDA product code EKE covers "Curette, Operative", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel.
Classification Details
- Product Code
- EKE
- Device Class
- Class I
- Regulation Number
- 872.4565
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No