The following data is part of a premarket notification filed by W. Keith Thornton, D.d.s. with the FDA for Toa.
| Device ID | K972061 |
| 510k Number | K972061 |
| Device Name: | TOA |
| Classification | Device, Anti-snoring |
| Applicant | W. KEITH THORNTON, D.D.S. 6131 LUTHER LANE, SUITE 208 Dallas, TX 75225 |
| Contact | W. Keith Thornton |
| Correspondent | W. Keith Thornton W. KEITH THORNTON, D.D.S. 6131 LUTHER LANE, SUITE 208 Dallas, TX 75225 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-03 |
| Decision Date | 1997-08-21 |
| Summary: | summary |