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FDA 510(k)

FOLDING CRUTCH

K-Number: K800237 · 1980-02-22

ApplicantHusa Folding Crutch Co., Inc.
Decision Date1980-02-22
Product CodeIPR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FOLDING CRUTCH is the device name listed in this FDA 510(k) record. The listed applicant is Husa Folding Crutch Co., Inc.. It received FDA 510(k) clearance on 1980-02-22 under 510(k) number K800237. The device is classified under product code IPR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOLDING CRUTCH?

FOLDING CRUTCH is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is Husa Folding Crutch Co., Inc.. The 510(k) number is K800237.

When did FOLDING CRUTCH receive FDA 510(k) clearance?

FOLDING CRUTCH received FDA 510(k) clearance on 1980-02-22, under 510(k) number K800237.

Who is the listed applicant for FOLDING CRUTCH?

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

What is the FDA product code for FOLDING CRUTCH?

The FDA product code for FOLDING CRUTCH is IPR.

Related Clinical Trials

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Related Devices (Code: IPR)

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.

K821403LIGHT WEIGHT ALUMINUM CRUTCHESManuco Manufacturing Co., Inc.K790557CRUTCHMaddak, Inc.K770146SWIVEL HEAD ADJUSTABLE CRUTCHMaddak, Inc.

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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