NFQ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Dental Sonography, For Monitoring Jaw Sounds
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.2050
- Medical specialty
- Dental
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ESG-1 ELECTROSONOGRAM (ESG-1) (K970116) | Myo-Tronics, Inc. | 1997-04-02 |
| SONOPAK/QS, SONOPAK (K905657) | Bioresearch | 1991-05-15 |
| ELECTROSONOGRAM ESG-1 (K905449) | Myo-Tronics, Inc. | 1991-04-26 |
| ARTHROPHONOMETER (K862286) | Arthrotek, Inc. | 1987-01-07 |
Track NFQ automatically
Every clearance here is in the API, with alerts when new ones post.