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BARD INLAY LUBRICIOUS DOUBLE PIGTAIL URETERAL STENT WITH SUTURE (HEREINAFTER REFERRED TO AS BARD LUBRICIOUS URETERAL STE

K983498 Class II Abbreviated
Decision Date
1998-12-15
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K983498
Product Code FAD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4620
Decision Date 1998-12-15
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARD INLAY LUBRICIOUS DOUBLE PIGTAIL URETERAL STENT WITH SUTURE (HEREINAFTER REFERRED TO AS BARD LUBRICIOUS URETERAL STE received FDA 510(k) clearance under submission number K983498, sponsored by C.R. Bard, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1998-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code FAD and 21 CFR 876.4620, within the Gastroenterology, Urology review panel as a Class II device.