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FDA 510(k)

TRAXX ELECTRIC WHEELCHAIR

K-Number: K022194 · 2002-10-29

ApplicantCrossroads Distribution Company, LLC
Decision Date2002-10-29
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRAXX ELECTRIC WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Crossroads Distribution Company, LLC. It received FDA 510(k) clearance on 2002-10-29 under 510(k) number K022194. 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 TRAXX ELECTRIC WHEELCHAIR?

TRAXX ELECTRIC WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-10-29. The listed applicant is Crossroads Distribution Company, LLC. The 510(k) number is K022194.

When did TRAXX ELECTRIC WHEELCHAIR receive FDA 510(k) clearance?

TRAXX ELECTRIC WHEELCHAIR received FDA 510(k) clearance on 2002-10-29, under 510(k) number K022194.

Who is the listed applicant for TRAXX ELECTRIC WHEELCHAIR?

The FDA 510(k) record lists Crossroads Distribution Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRAXX ELECTRIC WHEELCHAIR?

The FDA product code for TRAXX ELECTRIC 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

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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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