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FDA 510(k)

THE ENDURO

K-Number: K851227 · 1985-07-01

ApplicantWheel Ring, Inc.
Decision Date1985-07-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE ENDURO is the device name listed in this FDA 510(k) record. The listed applicant is Wheel Ring, Inc.. It received FDA 510(k) clearance on 1985-07-01 under 510(k) number K851227. 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 THE ENDURO?

THE ENDURO is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Wheel Ring, Inc.. The 510(k) number is K851227.

When did THE ENDURO receive FDA 510(k) clearance?

THE ENDURO received FDA 510(k) clearance on 1985-07-01, under 510(k) number K851227.

Who is the listed applicant for THE ENDURO?

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

What is the FDA product code for THE ENDURO?

The FDA product code for THE ENDURO 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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