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FDA 510(k)

UNIVERSAL SURGICAL INSTRUMENT HOLDER

K-Number: K924713 · 1993-05-17

Decision Date1993-05-17
Product CodeFWW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL SURGICAL INSTRUMENT HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K924713. The device is classified under product code FWW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL SURGICAL INSTRUMENT HOLDER?

UNIVERSAL SURGICAL INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K924713.

When did UNIVERSAL SURGICAL INSTRUMENT HOLDER receive FDA 510(k) clearance?

UNIVERSAL SURGICAL INSTRUMENT HOLDER received FDA 510(k) clearance on 1993-05-17, under 510(k) number K924713.

Who is the listed applicant for UNIVERSAL SURGICAL INSTRUMENT HOLDER?

The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL SURGICAL INSTRUMENT HOLDER?

The FDA product code for UNIVERSAL SURGICAL INSTRUMENT HOLDER is FWW.

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.

Other records listing T. Korossurgical Instruments Corp. as applicant

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.

View all 27 devices →

Related Devices (Code: FWW)

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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