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FDA 510(k)

STANDARD WHEELCHAIRS

K-Number: K860521 · 1986-03-10

ApplicantFormotion, Inc.
Decision Date1986-03-10
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STANDARD WHEELCHAIRS is the device name listed in this FDA 510(k) record. The listed applicant is Formotion, Inc.. It received FDA 510(k) clearance on 1986-03-10 under 510(k) number K860521. 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 STANDARD WHEELCHAIRS?

STANDARD WHEELCHAIRS is a medical device that received FDA 510(k) clearance on 1986-03-10. The listed applicant is Formotion, Inc.. The 510(k) number is K860521.

When did STANDARD WHEELCHAIRS receive FDA 510(k) clearance?

STANDARD WHEELCHAIRS received FDA 510(k) clearance on 1986-03-10, under 510(k) number K860521.

Who is the listed applicant for STANDARD WHEELCHAIRS?

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

What is the FDA product code for STANDARD WHEELCHAIRS?

The FDA product code for STANDARD WHEELCHAIRS 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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