RadiForce MX317W
K-Number: K233465 · 2023-12-21
ApplicantEizo Corporation
Decision Date2023-12-21
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RadiForce MX317W is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2023-12-21 under approval number K233465. 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 MX317W?
RadiForce MX317W is a medical device that received FDA 510(k) clearance on 2023-12-21. It is manufactured by Eizo Corporation. The 510(k) number is K233465.
When was RadiForce MX317W approved by the FDA?
RadiForce MX317W received FDA 510(k) clearance on 2023-12-21, under approval number K233465.
What company makes RadiForce MX317W?
RadiForce MX317W is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce MX317W?
The FDA product code for RadiForce MX317W 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.