RadiForce RX270
K-Number: K223768 · 2023-04-20
ApplicantEizo Corporation
Decision Date2023-04-20
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RadiForce RX270 is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2023-04-20 under approval number K223768. 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 RX270?
RadiForce RX270 is a medical device that received FDA 510(k) clearance on 2023-04-20. It is manufactured by Eizo Corporation. The 510(k) number is K223768.
When was RadiForce RX270 approved by the FDA?
RadiForce RX270 received FDA 510(k) clearance on 2023-04-20, under approval number K223768.
What company makes RadiForce RX270?
RadiForce RX270 is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce RX270?
The FDA product code for RadiForce RX270 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.