The following data is part of a premarket notification filed by Mission Dental, Inc. with the FDA for Dental Mouthprop (bite Block).
| Device ID | K792157 |
| 510k Number | K792157 |
| Device Name: | DENTAL MOUTHPROP (BITE BLOCK) |
| Classification | Block, Bite |
| Applicant | MISSION DENTAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JXL |
| CFR Regulation Number | 882.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-29 |
| Decision Date | 1979-11-13 |