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FDA 510(k)

EndoGator Endoscopy Irrigation Tubing

K-Number: K220395 · 2022-03-11

ApplicantSTERIS Corporation
Decision Date2022-03-11
Product CodeFEQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EndoGator Endoscopy Irrigation Tubing is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2022-03-11 under approval number K220395. The device is classified under product code FEQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EndoGator Endoscopy Irrigation Tubing?

EndoGator Endoscopy Irrigation Tubing is a medical device that received FDA 510(k) clearance on 2022-03-11. It is manufactured by STERIS Corporation. The 510(k) number is K220395.

When was EndoGator Endoscopy Irrigation Tubing approved by the FDA?

EndoGator Endoscopy Irrigation Tubing received FDA 510(k) clearance on 2022-03-11, under approval number K220395.

What company makes EndoGator Endoscopy Irrigation Tubing?

EndoGator Endoscopy Irrigation Tubing is manufactured by STERIS Corporation.

What is the FDA product code for EndoGator Endoscopy Irrigation Tubing?

The FDA product code for EndoGator Endoscopy Irrigation Tubing is FEQ.

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Related Devices (Code: FEQ)

K162152Erbe’s CO2 Tubing/Cap SetsErbe USA, Inc. K161482EndoChoice Water Bottle Cap Irrigation SystemEndochoice, Inc. K153588EndoChoice Water Bottle Cap SystemEndochoice, Inc. K163424AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINONUnited State Endoscopy Group, Inc. K182258AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - FujifilmUnited States Endoscopy Group, Inc. K173650AquaShield System CO2- FujifilmUnited States Endoscopy Group, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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