The following data is part of a premarket notification filed by Leonard Medical, Inc. with the FDA for Mandible Manipulator.
| Device ID | K884308 |
| 510k Number | K884308 |
| Device Name: | MANDIBLE MANIPULATOR |
| Classification | Burnisher, Operative |
| Applicant | LEONARD MEDICAL, INC. 1464 HOLCOMB RD. Huntingdon Valley, PA 19006 |
| Contact | Leonard J Bonnell |
| Correspondent | Leonard J Bonnell LEONARD MEDICAL, INC. 1464 HOLCOMB RD. Huntingdon Valley, PA 19006 |
| Product Code | EKJ |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-13 |
| Decision Date | 1989-03-31 |