meddevicedb.com FDA Device Reference

LOPEZ VALVE WITH NG SUMP TUBE

K921104 Class II Traditional
Decision Date
1992-10-26
Sponsor / Applicant
Icu Medical, Inc.

Technical Specification

510(k) Submission ID K921104
Product Code FEG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1992-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOPEZ VALVE WITH NG SUMP TUBE received FDA 510(k) clearance under submission number K921104, sponsored by Icu Medical, 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 1992-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code FEG and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.