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FDA 510(k)

THE LIBERATOR WHEELCHAIR

K-Number: K010859 · 2001-04-05

ApplicantLiberator Wheelchairs, Inc.
Decision Date2001-04-05
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE LIBERATOR WHEELCHAIR 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 2001-04-05 under 510(k) number K010859. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE LIBERATOR WHEELCHAIR?

THE LIBERATOR WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2001-04-05. The listed applicant is Liberator Wheelchairs, Inc.. The 510(k) number is K010859.

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

THE LIBERATOR WHEELCHAIR received FDA 510(k) clearance on 2001-04-05, under 510(k) number K010859.

Who is the listed applicant for THE LIBERATOR WHEELCHAIR?

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 WHEELCHAIR?

The FDA product code for THE LIBERATOR WHEELCHAIR is ITI.

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.

K984391THE LIBERATOR

Related Devices (Code: ITI)

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

Official Source

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

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