meddevicedb.com FDA Device Reference

andorate Suction Valve, andorate Air/Water Valve

K213095 Class II Traditional
Decision Date
2022-01-12
Sponsor / Applicant
Ga Health Company Limited

Technical Specification

510(k) Submission ID K213095
Product Code ODC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2022-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

andorate Suction Valve, andorate Air/Water Valve received FDA 510(k) clearance under submission number K213095, sponsored by Ga Health Company Limited. 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 2022-01-12.

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.