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FDA 510(k)

REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR

K-Number: K926583 · 1993-08-06

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

Device Summary

REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR 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 1993-08-06 under 510(k) number K926583. 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 REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR?

REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K926583.

When did REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR receive FDA 510(k) clearance?

REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR received FDA 510(k) clearance on 1993-08-06, under 510(k) number K926583.

Who is the listed applicant for REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR?

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 REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR?

The FDA product code for REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR 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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