meddevicedb.com FDA Device Reference

HIGH FLOW INSUFFLATION UNIT UHI-4

K110294 Class II Traditional
Decision Date
2011-11-18
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K110294
Product Code HIF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1730
Decision Date 2011-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH FLOW INSUFFLATION UNIT UHI-4 received FDA 510(k) clearance under submission number K110294, sponsored by Olympus Medical Systems Corporation. 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 2011-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code HIF and 21 CFR 884.1730, within the Obstetrics/Gynecology review panel as a Class II device.