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VANGUARD REPROCESSED DILATING TIP AND BLUNT TROCARS

K043253 Class II Traditional
Decision Date
2005-04-08
Sponsor / Applicant
Vanguard Medical Concepts, Inc.

Technical Specification

510(k) Submission ID K043253
Product Code NLM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2005-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VANGUARD REPROCESSED DILATING TIP AND BLUNT TROCARS received FDA 510(k) clearance under submission number K043253, sponsored by Vanguard Medical Concepts, 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 2005-04-08.

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.