FUJIFILM Distal End Cap
K-Number: K203028 · 2020-10-30
ApplicantFujifilm Corporation
Decision Date2020-10-30
Product CodeFDT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
FUJIFILM Distal End Cap is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2020-10-30 under approval number K203028. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FUJIFILM Distal End Cap?
FUJIFILM Distal End Cap is a medical device that received FDA 510(k) clearance on 2020-10-30. It is manufactured by Fujifilm Corporation. The 510(k) number is K203028.
When was FUJIFILM Distal End Cap approved by the FDA?
FUJIFILM Distal End Cap received FDA 510(k) clearance on 2020-10-30, under approval number K203028.
What company makes FUJIFILM Distal End Cap?
FUJIFILM Distal End Cap is manufactured by Fujifilm Corporation.
What is the FDA product code for FUJIFILM Distal End Cap?
The FDA product code for FUJIFILM Distal End Cap is FDT.
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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.