THE LIBERATOR— 510(k) K984391

Substantially Equivalent

Liberator Wheelchairs, Inc.

FDA 510(k) clearance K984391 for THE LIBERATOR, Substantially Equivalent on 1999-09-03. Applicant: Liberator Wheelchairs, Inc.. Device class: 2.

Clearance details

Applicant: Liberator Wheelchairs, Inc.
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 1998-12-08
Decision date: 1999-09-03
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IPL

K243783 — Walking rehabilitation training electric wheelchair (ZW518)2025-03-12
K202728 — Action Trackchair Hawk2022-02-10
K203761 — ParaMotion2022-01-21
K191334 — Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD082020-05-29
K190682 — Explorer Mini2020-02-27

More clearances from Liberator Wheelchairs, Inc.

K010859 — THE LIBERATOR WHEELCHAIR2001-04-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.