The following data is part of a premarket notification filed by Liberator Wheelchairs, Inc. with the FDA for The Liberator.
| Device ID | K984391 |
| 510k Number | K984391 |
| Device Name: | THE LIBERATOR |
| Classification | Wheelchair, Standup |
| Applicant | LIBERATOR WHEELCHAIRS, INC. 7525 PARKWOOD LN. Ft. Worth, TX 76133 |
| Contact | Bonnie Bromley |
| Correspondent | Bonnie Bromley LIBERATOR WHEELCHAIRS, INC. 7525 PARKWOOD LN. Ft. Worth, TX 76133 |
| Product Code | IPL |
| CFR Regulation Number | 890.3900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-12-08 |
| Decision Date | 1999-09-03 |