RadiForce MX317W-PA
K-Number: K242545 · 2025-05-23
ApplicantEizo Corporation
Decision Date2025-05-23
Product CodePZZ
Advisory CommitteePA
DecisionSubstantially Equivalent
Device Summary
RadiForce MX317W-PA is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2025-05-23 under approval number K242545. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RadiForce MX317W-PA?
RadiForce MX317W-PA is a medical device that received FDA 510(k) clearance on 2025-05-23. It is manufactured by Eizo Corporation. The 510(k) number is K242545.
When was RadiForce MX317W-PA approved by the FDA?
RadiForce MX317W-PA received FDA 510(k) clearance on 2025-05-23, under approval number K242545.
What company makes RadiForce MX317W-PA?
RadiForce MX317W-PA is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce MX317W-PA?
The FDA product code for RadiForce MX317W-PA is PZZ.
Other Devices by Eizo Corporation
Related Devices (Code: PZZ)
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.