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FDA 510(k)

LANDEEZ ALL-TERRAIN WHEELCHAIR

K-Number: K954261 · 1995-10-13

Decision Date1995-10-13
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LANDEEZ ALL-TERRAIN WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Natural Access. It received FDA 510(k) clearance on 1995-10-13 under 510(k) number K954261. 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 LANDEEZ ALL-TERRAIN WHEELCHAIR?

LANDEEZ ALL-TERRAIN WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1995-10-13. The listed applicant is Natural Access. The 510(k) number is K954261.

When did LANDEEZ ALL-TERRAIN WHEELCHAIR receive FDA 510(k) clearance?

LANDEEZ ALL-TERRAIN WHEELCHAIR received FDA 510(k) clearance on 1995-10-13, under 510(k) number K954261.

Who is the listed applicant for LANDEEZ ALL-TERRAIN WHEELCHAIR?

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

What is the FDA product code for LANDEEZ ALL-TERRAIN WHEELCHAIR?

The FDA product code for LANDEEZ ALL-TERRAIN WHEELCHAIR is IOR.

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.

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.

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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