Fujifilm Video Colonoscope Model EC-600WL V2
K-Number: K160196 · 2016-02-23
ApplicantFujifilm Medical Systems U.S.A, Inc.
Decision Date2016-02-23
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Fujifilm Video Colonoscope Model EC-600WL V2 is a medical device manufactured by Fujifilm Medical Systems U.S.A, Inc.. It received FDA 510(k) clearance on 2016-02-23 under approval number K160196. 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 Video Colonoscope Model EC-600WL V2?
Fujifilm Video Colonoscope Model EC-600WL V2 is a medical device that received FDA 510(k) clearance on 2016-02-23. It is manufactured by Fujifilm Medical Systems U.S.A, Inc.. The 510(k) number is K160196.
When was Fujifilm Video Colonoscope Model EC-600WL V2 approved by the FDA?
Fujifilm Video Colonoscope Model EC-600WL V2 received FDA 510(k) clearance on 2016-02-23, under approval number K160196.
What company makes Fujifilm Video Colonoscope Model EC-600WL V2?
Fujifilm Video Colonoscope Model EC-600WL V2 is manufactured by Fujifilm Medical Systems U.S.A, Inc..
What is the FDA product code for Fujifilm Video Colonoscope Model EC-600WL V2?
The FDA product code for Fujifilm Video Colonoscope Model EC-600WL V2 is FDF.
Related Clinical Trials
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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.