meddevicedb.com FDA Device Reference

FST CATH - UI USRODYNAMIC CATH INTRODUCER SYSTEM

K913721 Class II Traditional
Decision Date
1991-10-08
Sponsor / Applicant
Fiberoptic Sensor Technlogies, Inc.

Technical Specification

510(k) Submission ID K913721
Product Code FEN
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1620
Decision Date 1991-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FST CATH - UI USRODYNAMIC CATH INTRODUCER SYSTEM received FDA 510(k) clearance under submission number K913721, sponsored by Fiberoptic Sensor Technlogies, 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 1991-10-08.

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.