RadiForce MX217
K-Number: K230684 · 2023-05-12
ApplicantEizo Corporation
Decision Date2023-05-12
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RadiForce MX217 is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2023-05-12 under approval number K230684. 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 MX217?
RadiForce MX217 is a medical device that received FDA 510(k) clearance on 2023-05-12. It is manufactured by Eizo Corporation. The 510(k) number is K230684.
When was RadiForce MX217 approved by the FDA?
RadiForce MX217 received FDA 510(k) clearance on 2023-05-12, under approval number K230684.
What company makes RadiForce MX217?
RadiForce MX217 is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce MX217?
The FDA product code for RadiForce MX217 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.