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SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES

K024011 Class II Traditional
Decision Date
2002-12-19
Sponsor / Applicant
Surgical Instruments Service and Savings, Inc.

Technical Specification

510(k) Submission ID K024011
Product Code NLU
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2002-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES received FDA 510(k) clearance under submission number K024011, sponsored by Surgical Instruments Service and Savings, Inc.. 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 2002-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code NLU and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.