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ENDOSCOPIC OR THORASCOPIC FORCEPS

K931259 Class II Traditional
Decision Date
1993-06-08
Sponsor / Applicant
T. Korossurgical Instruments Corp.

Technical Specification

510(k) Submission ID K931259
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1993-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPIC OR THORASCOPIC FORCEPS received FDA 510(k) clearance under submission number K931259, sponsored by T. Korossurgical Instruments Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1993-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.