SCENARIA View
K-Number: K213829 · 2022-05-23
ApplicantFujifilm Healthcare Corporation
Decision Date2022-05-23
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
SCENARIA View is a medical device manufactured by Fujifilm Healthcare Corporation. It received FDA 510(k) clearance on 2022-05-23 under approval number K213829. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SCENARIA View?
SCENARIA View is a medical device that received FDA 510(k) clearance on 2022-05-23. It is manufactured by Fujifilm Healthcare Corporation. The 510(k) number is K213829.
When was SCENARIA View approved by the FDA?
SCENARIA View received FDA 510(k) clearance on 2022-05-23, under approval number K213829.
What company makes SCENARIA View?
SCENARIA View is manufactured by Fujifilm Healthcare Corporation.
What is the FDA product code for SCENARIA View?
The FDA product code for SCENARIA View is JAK.
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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.