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FDA 510(k)

CHEYENNE MODEL 107A WHEELCHAIR

K-Number: K870292 · 1987-02-10

ApplicantRedman, Inc.
Decision Date1987-02-10
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHEYENNE MODEL 107A WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870292. 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 CHEYENNE MODEL 107A WHEELCHAIR?

CHEYENNE MODEL 107A WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Redman, Inc.. The 510(k) number is K870292.

When did CHEYENNE MODEL 107A WHEELCHAIR receive FDA 510(k) clearance?

CHEYENNE MODEL 107A WHEELCHAIR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870292.

Who is the listed applicant for CHEYENNE MODEL 107A WHEELCHAIR?

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

What is the FDA product code for CHEYENNE MODEL 107A WHEELCHAIR?

The FDA product code for CHEYENNE MODEL 107A WHEELCHAIR is IOR.

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Other records listing Redman, Inc. as applicant

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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