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FDA 510(k)

HAVERICH ORTHOPAEDIC CYCLES

K-Number: K932795 · 1993-07-22

Decision Date1993-07-22
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAVERICH ORTHOPAEDIC CYCLES is the device name listed in this FDA 510(k) record. The listed applicant is Haverich Ortho-Sport (Usa), Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932795. 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 HAVERICH ORTHOPAEDIC CYCLES?

HAVERICH ORTHOPAEDIC CYCLES is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Haverich Ortho-Sport (Usa), Inc.. The 510(k) number is K932795.

When did HAVERICH ORTHOPAEDIC CYCLES receive FDA 510(k) clearance?

HAVERICH ORTHOPAEDIC CYCLES received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932795.

Who is the listed applicant for HAVERICH ORTHOPAEDIC CYCLES?

The FDA 510(k) record lists Haverich Ortho-Sport (Usa), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAVERICH ORTHOPAEDIC CYCLES?

The FDA product code for HAVERICH ORTHOPAEDIC CYCLES 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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