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FDA 510(k)

THE TERMINATOR

K-Number: K922535 · 1992-07-24

Decision Date1992-07-24
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE TERMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Top End Wheelchair Sports, Inc.. It received FDA 510(k) clearance on 1992-07-24 under 510(k) number K922535. 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 TERMINATOR?

THE TERMINATOR is a medical device that received FDA 510(k) clearance on 1992-07-24. The listed applicant is Top End Wheelchair Sports, Inc.. The 510(k) number is K922535.

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

THE TERMINATOR received FDA 510(k) clearance on 1992-07-24, under 510(k) number K922535.

Who is the listed applicant for THE TERMINATOR?

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

What is the FDA product code for THE TERMINATOR?

The FDA product code for THE TERMINATOR 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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