Water Bottle Cap Irrigaton System

FDA 510(k) K120862 · Endochoice, Inc.

Substantially Equivalent

510(k) numberK120862

Submission

Device name
Water Bottle Cap Irrigaton System
Applicant
Endochoice, Inc.
Alpharetta, GA, US
Received
March 22, 2012
Decision date
November 27, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FEQ – Pump, Air, Non-Manual, For Endoscope
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

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K162152Erbe’s CO2 Tubing/Cap SetsFEQ · Special Erbe USA, Inc.08/31/2016SE
K161482EndoChoice Water Bottle Cap Irrigation SystemFEQ · Special Endochoice, Inc.06/27/2016SE
K153588EndoChoice Water Bottle Cap SystemFEQ · Special Endochoice, Inc.02/24/2016SE
K153362AquaShield system CO2, AquaShield system-PENTAXFEQ · Special United States Endoscopy Group, Inc.12/16/2015SE
K142155Endochoice Water Bottle Cap SystemFEQ · Traditional Endochoice, Inc.01/20/2015SE

More from Endochoice, Inc.

510(k)DeviceDecision
K160275Fuse Endoscopic System with FuseBox ProcessorPEA · Traditional 08/01/2016SE
K161482EndoChoice Water Bottle Cap Irrigation SystemFEQ · Special 06/27/2016SE
K161167Seal Single-Use Biopsy ValveOCX · Special 05/26/2016SE
K160403SmartStart Air/Water and Suction ValvesODC · Traditional 05/19/2016SE
K153588EndoChoice Water Bottle Cap SystemFEQ · Special 02/24/2016SE
K151475EndoChoice Select Injection NeedleFBK · Traditional 02/08/2016SE
K152182Fuse Gastroscopy SystemFDS · Special 12/10/2015SE
K152580rescuenetFDI · Traditional 11/03/2015SE
K142155Endochoice Water Bottle Cap SystemFEQ · Traditional 01/20/2015SE
K140472Bonastent Tracheal / BronchialJCT · Traditional 10/17/2014SE

Questions and answers

When was Water Bottle Cap Irrigaton System cleared by the FDA?

Water Bottle Cap Irrigaton System (K120862) received a 510(k) decision of Substantially Equivalent on November 27, 2012, 250 days after the submission was received.

What is the product code of K120862?

The FDA product code is FEQ – Pump, Air, Non-Manual, For Endoscope, a Class II (moderate risk) device regulated under 21 CFR 876.1500.