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FDA 510(k)

FX 222-02 POWERED WHEELCHAIR

K-Number: K110036 · 2011-03-28

ApplicantLanzhou Wanli Aviation Electromechanical, Inc.
Decision Date2011-03-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FX 222-02 POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Lanzhou Wanli Aviation Electromechanical, Inc.. It received FDA 510(k) clearance on 2011-03-28 under 510(k) number K110036. 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 FX 222-02 POWERED WHEELCHAIR?

FX 222-02 POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2011-03-28. The listed applicant is Lanzhou Wanli Aviation Electromechanical, Inc.. The 510(k) number is K110036.

When did FX 222-02 POWERED WHEELCHAIR receive FDA 510(k) clearance?

FX 222-02 POWERED WHEELCHAIR received FDA 510(k) clearance on 2011-03-28, under 510(k) number K110036.

Who is the listed applicant for FX 222-02 POWERED WHEELCHAIR?

The FDA 510(k) record lists Lanzhou Wanli Aviation Electromechanical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FX 222-02 POWERED WHEELCHAIR?

The FDA product code for FX 222-02 POWERED WHEELCHAIR is ITI.

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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.

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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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