The following data is part of a premarket notification filed by Dasoft Partners with the FDA for Advanced Dental Appliance.
| Device ID | K203462 |
| 510k Number | K203462 |
| Device Name: | Advanced Dental Appliance |
| Classification | Device, Anti-snoring |
| Applicant | DaSoft Partners 4079 Governor Drive #111 San Diego, CA 92122 |
| Contact | Dante Togliatti |
| Correspondent | Kimberly Lane J Blane, LLC 980 N Sinagua Heights Dr Flagstaff, AZ 86004 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-11-24 |
| Decision Date | 2021-02-19 |