Fujifilm Ultrasonic Processor
K-Number: K200850 · 2020-07-06
ApplicantFujifilm Corporation
Decision Date2020-07-06
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Fujifilm Ultrasonic Processor is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2020-07-06 under approval number K200850. 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 Fujifilm Ultrasonic Processor?
Fujifilm Ultrasonic Processor is a medical device that received FDA 510(k) clearance on 2020-07-06. It is manufactured by Fujifilm Corporation. The 510(k) number is K200850.
When was Fujifilm Ultrasonic Processor approved by the FDA?
Fujifilm Ultrasonic Processor received FDA 510(k) clearance on 2020-07-06, under approval number K200850.
What company makes Fujifilm Ultrasonic Processor?
Fujifilm Ultrasonic Processor is manufactured by Fujifilm Corporation.
What is the FDA product code for Fujifilm Ultrasonic Processor?
The FDA product code for Fujifilm Ultrasonic Processor 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.