meddevicedb.com FDA Device Reference

UROPUMP TUBE & DAMPING CHAMGER

K953451 Class II Traditional
Decision Date
1995-10-05
Sponsor / Applicant
Life-Tech Intl., Inc.

Technical Specification

510(k) Submission ID K953451
Product Code FEN
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1620
Decision Date 1995-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UROPUMP TUBE & DAMPING CHAMGER received FDA 510(k) clearance under submission number K953451, sponsored by Life-Tech Intl., 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 1995-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code FEN and 21 CFR 876.1620, within the Gastroenterology, Urology review panel as a Class II device.