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FDA 510(k)

FUJIFILM Endoscope Model EC-760Z-V/L

K-Number: K192664 · 2019-11-20

ApplicantFujifilm Corporation
Decision Date2019-11-20
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EC-760Z-V/L is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2019-11-20 under approval number K192664. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJIFILM Endoscope Model EC-760Z-V/L?

FUJIFILM Endoscope Model EC-760Z-V/L is a medical device that received FDA 510(k) clearance on 2019-11-20. It is manufactured by Fujifilm Corporation. The 510(k) number is K192664.

When was FUJIFILM Endoscope Model EC-760Z-V/L approved by the FDA?

FUJIFILM Endoscope Model EC-760Z-V/L received FDA 510(k) clearance on 2019-11-20, under approval number K192664.

What company makes FUJIFILM Endoscope Model EC-760Z-V/L?

FUJIFILM Endoscope Model EC-760Z-V/L is manufactured by Fujifilm Corporation.

What is the FDA product code for FUJIFILM Endoscope Model EC-760Z-V/L?

The FDA product code for FUJIFILM Endoscope Model EC-760Z-V/L is FDF.

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Related Devices (Code: FDF)

K162428DiLumen Endolumenal Interventional PlatformLumendi, LLC K162622Fujifilm Endoscope Models EC-600HL and EC-600LSFujifilm Medical Systems U.S.A, Inc. K160015Pure VuMotus GI Medical Technologies , Ltd. K161355invendoscopy E200 SystemInvendo Medical GmbH K161791Aer-O-Scope Colonoscope SystemGi View , Ltd. K160356Third Eye Panoramic Auxiliary Endoscopy System - ResposableAvantis Medical Systems, 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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