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URETHRALPRESSURE PROFILE CATHETER

K915484 Class II Traditional
Decision Date
1992-02-24
Sponsor / Applicant
Life-Tech Intl., Inc.

Technical Specification

510(k) Submission ID K915484
Product Code FAP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1620
Decision Date 1992-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URETHRALPRESSURE PROFILE CATHETER received FDA 510(k) clearance under submission number K915484, 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 1992-02-24.

Classification & Regulation

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