meddevicedb.com FDA Device Reference

ENDOCHOICE WATER BOTTLE CAP SYSTEM

K142155 Class II Traditional
Decision Date
2015-01-20
Sponsor / Applicant
Endochoice, Inc.

Technical Specification

510(k) Submission ID K142155
Product Code FEQ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2015-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOCHOICE WATER BOTTLE CAP SYSTEM received FDA 510(k) clearance under submission number K142155, sponsored by Endochoice, 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 2015-01-20.

Classification & Regulation

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