meddevicedb.com FDA Device Reference

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD

K863168 Class II Traditional
Decision Date
1986-10-24
Sponsor / Applicant
Life-Tech Intl., Inc.

Technical Specification

510(k) Submission ID K863168
Product Code FAP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1620
Decision Date 1986-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD received FDA 510(k) clearance under submission number K863168, 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 1986-10-24.

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.