meddevicedb.com FDA Device Reference

GASTRIC LAVAGE VALVE

K990365 Class II Traditional
Decision Date
2000-07-26
Sponsor / Applicant
T-Med Vac Corporation

Technical Specification

510(k) Submission ID K990365
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2000-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GASTRIC LAVAGE VALVE received FDA 510(k) clearance under submission number K990365, sponsored by T-Med Vac Corporation. 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 2000-07-26.

Classification & Regulation

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