FDA Product Code
FDA Product Code EKQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Dental
- 21 CFR Citation
- 872.4565
510(k) Clearances — 2 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K832378 | VIBRATORY ENDODONTIC SYSTEM | Syntex Dental Products, Inc. | 1983-10-04 | Traditional | PDF ↗ |
| K801463 | OJ-1 ENDODONIC ROOT CANAL FILE HOLDER | Almore Intl., Inc. | 1980-07-21 | Traditional | PDF ↗ |
Product code EKQ · Class I · Dental. Data: openFDA.