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FDA 510(k)

POWERED WHEELCHAIR, MODEL FR168W

K-Number: K033370 · 2003-11-28

ApplicantFreerider Corp
Decision Date2003-11-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWERED WHEELCHAIR, MODEL FR168W is the device name listed in this FDA 510(k) record. The listed applicant is Freerider Corp. It received FDA 510(k) clearance on 2003-11-28 under 510(k) number K033370. 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 POWERED WHEELCHAIR, MODEL FR168W?

POWERED WHEELCHAIR, MODEL FR168W is a medical device that received FDA 510(k) clearance on 2003-11-28. The listed applicant is Freerider Corp. The 510(k) number is K033370.

When did POWERED WHEELCHAIR, MODEL FR168W receive FDA 510(k) clearance?

POWERED WHEELCHAIR, MODEL FR168W received FDA 510(k) clearance on 2003-11-28, under 510(k) number K033370.

Who is the listed applicant for POWERED WHEELCHAIR, MODEL FR168W?

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

What is the FDA product code for POWERED WHEELCHAIR, MODEL FR168W?

The FDA product code for POWERED WHEELCHAIR, MODEL FR168W 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

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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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