EKQ — Preparer, Root Canal Endodontic Class I
FDA Device Classification
Classification Details
- Product Code
- EKQ
- 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 |
|---|
| K832378 | syntex dental products | VIBRATORY ENDODONTIC SYSTEM | October 4, 1983 |
| K801463 | almore intl | OJ-1 ENDODONIC ROOT CANAL FILE HOLDER | July 21, 1980 |