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FDA 510(k)

INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91

K-Number: K021680 · 2002-06-18

Decision Date2002-06-18
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2002-06-18 under 510(k) number K021680. 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 INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91?

INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 is a medical device that received FDA 510(k) clearance on 2002-06-18. The listed applicant is Invacare Corp.. The 510(k) number is K021680.

When did INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 receive FDA 510(k) clearance?

INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 received FDA 510(k) clearance on 2002-06-18, under 510(k) number K021680.

Who is the listed applicant for INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91?

The FDA product code for INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 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.

Other records listing Invacare Corp. 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.

View all 111 devices →

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.

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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