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ANGIODYNAMICS TOTAL ABSCESSION BILIARY DRAINAGE CATHETER

K060023 Class II Special
Decision Date
2006-03-09
Sponsor / Applicant
AngioDynamics, Inc.

Technical Specification

510(k) Submission ID K060023
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2006-03-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANGIODYNAMICS TOTAL ABSCESSION BILIARY DRAINAGE CATHETER received FDA 510(k) clearance under submission number K060023, sponsored by AngioDynamics, 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 2006-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.