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REPROCESSED TROCARS AND CANNULAS

K012644 Class II Traditional
Decision Date
2002-07-29
Sponsor / Applicant
Surgical Instruments Service and Savings, Inc.

Technical Specification

510(k) Submission ID K012644
Product Code NLM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED TROCARS AND CANNULAS received FDA 510(k) clearance under submission number K012644, 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 2002-07-29.

Classification & Regulation

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