meddevicedb.com FDA Device Reference

Bio Guard Air/Water & Suction Valves

K192059 Class II Special
Decision Date
2019-09-17
Sponsor / Applicant
United States Endoscopy Group, Inc.

Technical Specification

510(k) Submission ID K192059
Product Code ODC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2019-09-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bio Guard Air/Water & Suction Valves received FDA 510(k) clearance under submission number K192059, sponsored by United States Endoscopy Group, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2019-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code ODC and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.