RadiForce MX243W
K-Number: K221136 · 2022-05-10
ApplicantEizo Corporation
Decision Date2022-05-10
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RadiForce MX243W is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2022-05-10 under approval number K221136. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RadiForce MX243W?
RadiForce MX243W is a medical device that received FDA 510(k) clearance on 2022-05-10. It is manufactured by Eizo Corporation. The 510(k) number is K221136.
When was RadiForce MX243W approved by the FDA?
RadiForce MX243W received FDA 510(k) clearance on 2022-05-10, under approval number K221136.
What company makes RadiForce MX243W?
RadiForce MX243W is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce MX243W?
The FDA product code for RadiForce MX243W is PGY.
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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.