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ENDOPATH DILATING TIP TROCAR, MODEL #512XD

K020428 Class II Special
Decision Date
2002-03-04
Sponsor / Applicant
Ethicon Endo-Surgery, Inc.

Technical Specification

510(k) Submission ID K020428
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-03-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOPATH DILATING TIP TROCAR, MODEL #512XD received FDA 510(k) clearance under submission number K020428, sponsored by Ethicon Endo-Surgery, Inc.. 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 2002-03-04.

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.