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FDA 510(k)

X2000 TRADITIONAL WHEELCHAIR

K-Number: K951351 · 1995-04-26

ApplicantHomecrest Industries
Decision Date1995-04-26
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

X2000 TRADITIONAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Homecrest Industries. It received FDA 510(k) clearance on 1995-04-26 under 510(k) number K951351. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X2000 TRADITIONAL WHEELCHAIR?

X2000 TRADITIONAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1995-04-26. The listed applicant is Homecrest Industries. The 510(k) number is K951351.

When did X2000 TRADITIONAL WHEELCHAIR receive FDA 510(k) clearance?

X2000 TRADITIONAL WHEELCHAIR received FDA 510(k) clearance on 1995-04-26, under 510(k) number K951351.

Who is the listed applicant for X2000 TRADITIONAL WHEELCHAIR?

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

What is the FDA product code for X2000 TRADITIONAL WHEELCHAIR?

The FDA product code for X2000 TRADITIONAL WHEELCHAIR is IOR.

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Related Devices (Code: IOR)

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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