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UROPLASTY TCU PROSTATIC URETHROPLASTY CATHETER

K902585 Class II Traditional
Decision Date
1990-08-27
Sponsor / Applicant
Advanced Surgical Intervention, Inc.

Technical Specification

510(k) Submission ID K902585
Product Code KOE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5520
Decision Date 1990-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UROPLASTY TCU PROSTATIC URETHROPLASTY CATHETER received FDA 510(k) clearance under submission number K902585, sponsored by Advanced Surgical Intervention, 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 1990-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code KOE and 21 CFR 876.5520, within the Gastroenterology, Urology review panel as a Class II device.