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FDA 510(k)

THE LIBERATOR

K-Number: K984391 · 1999-09-03

ApplicantLiberator Wheelchairs, Inc.
Decision Date1999-09-03
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE LIBERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Liberator Wheelchairs, Inc.. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K984391. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE LIBERATOR?

THE LIBERATOR is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Liberator Wheelchairs, Inc.. The 510(k) number is K984391.

When did THE LIBERATOR receive FDA 510(k) clearance?

THE LIBERATOR received FDA 510(k) clearance on 1999-09-03, under 510(k) number K984391.

Who is the listed applicant for THE LIBERATOR?

The FDA 510(k) record lists Liberator Wheelchairs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE LIBERATOR?

The FDA product code for THE LIBERATOR is IPL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Liberator Wheelchairs, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K010859THE LIBERATOR WHEELCHAIR

Related Devices (Code: IPL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243783Walking rehabilitation training electric wheelchair (ZW518)Shenzhen Zuowei Technology Co., Ltd.K202728Action Trackchair HawkAction Manufacturing, Inc.K203761ParaMotionPowerbasetec GmbHK191334Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08Matia Robotics (Us), Inc.K190682Explorer MiniPermobil ABK191874F5 Corpus VSPermobil AB

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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