The following data is part of a premarket notification filed by John J. Navar, M.d. with the FDA for Movit Device.
| Device ID | K921710 |
| 510k Number | K921710 |
| Device Name: | MOVIT DEVICE |
| Classification | Cabinet, Table And Tray, Anesthesia |
| Applicant | JOHN J. NAVAR, M.D. 337 CLAREMORE Corpus Christi, TX 78412 |
| Product Code | BRY |
| CFR Regulation Number | 868.6100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-04-08 |
| Decision Date | 1992-06-29 |