meddevicedb.com FDA Device Reference

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX

K001597 Class II Special
Decision Date
2000-06-05
Sponsor / Applicant
Conmedcorp

Technical Specification

510(k) Submission ID K001597
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2000-06-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX received FDA 510(k) clearance under submission number K001597, sponsored by Conmedcorp. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2000-06-05.

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.