Endoscope Model EI-740D/S
K-Number: K210162 · 2021-04-09
ApplicantFujifilm Corporation
Decision Date2021-04-09
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Endoscope Model EI-740D/S is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2021-04-09 under approval number K210162. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Endoscope Model EI-740D/S?
Endoscope Model EI-740D/S is a medical device that received FDA 510(k) clearance on 2021-04-09. It is manufactured by Fujifilm Corporation. The 510(k) number is K210162.
When was Endoscope Model EI-740D/S approved by the FDA?
Endoscope Model EI-740D/S received FDA 510(k) clearance on 2021-04-09, under approval number K210162.
What company makes Endoscope Model EI-740D/S?
Endoscope Model EI-740D/S is manufactured by Fujifilm Corporation.
What is the FDA product code for Endoscope Model EI-740D/S?
The FDA product code for Endoscope Model EI-740D/S is FDS.
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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.