The following data is part of a premarket notification filed by Allen J. Moses, Dds, Ltd. with the FDA for The Moses Express Appliance.
| Device ID | K142651 |
| 510k Number | K142651 |
| Device Name: | The Moses Express Appliance |
| Classification | Device, Anti-snoring |
| Applicant | ALLEN J. MOSES, DDS, LTD. 233 S. WACKER DR. Chicago, IL 60606 |
| Contact | Allen J. Moses, Dds |
| Correspondent | Gloria Pacini GLORIA PACINI 233 S. WACKER DRIVE Chicago, IL 60606 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-18 |
| Decision Date | 2015-07-17 |