EKB — Explorer, Operative Class I
FDA Device Classification
Classification Details
- Product Code
- EKB
- 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 |
|---|
| K851724 | artiberia | 1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS | July 2, 1985 |
| K823914 | treace medical | EXPLORER TIP | January 21, 1983 |
| K821780 | pacific dental | BEACH EXPLORER NO. 23T.G. | July 6, 1982 |