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 |