meddevicedb.com FDA Device Reference

UC-2000 UTERINE CATHERIZATION SYSTEM

K791633 Class II Traditional
Decision Date
1979-09-17
Sponsor / Applicant
Life Support, Inc.

Technical Specification

510(k) Submission ID K791633
Product Code HFO
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2700
Decision Date 1979-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UC-2000 UTERINE CATHERIZATION SYSTEM received FDA 510(k) clearance under submission number K791633, sponsored by Life Support, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1979-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code HFO and 21 CFR 884.2700, within the Obstetrics/Gynecology review panel as a Class II device.