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FDA 510(k)

ENDOSCOPIC OR THORASCOPIC FORCEPS

K-Number: K931259 · 1993-06-08

ApplicantT. Korossurgical Instruments Corp.
Decision Date1993-06-08
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC OR THORASCOPIC FORCEPS 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 1993-06-08 under 510(k) number K931259. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC OR THORASCOPIC FORCEPS?

ENDOSCOPIC OR THORASCOPIC FORCEPS is a medical device that received FDA 510(k) clearance on 1993-06-08. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K931259.

When did ENDOSCOPIC OR THORASCOPIC FORCEPS receive FDA 510(k) clearance?

ENDOSCOPIC OR THORASCOPIC FORCEPS received FDA 510(k) clearance on 1993-06-08, under 510(k) number K931259.

Who is the listed applicant for ENDOSCOPIC OR THORASCOPIC FORCEPS?

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 ENDOSCOPIC OR THORASCOPIC FORCEPS?

The FDA product code for ENDOSCOPIC OR THORASCOPIC FORCEPS is GCJ.

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Other records listing T. Korossurgical Instruments Corp. as applicant

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Related Devices (Code: GCJ)

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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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