RadiForce MX315W
K-Number: K170949 · 2017-04-27
ApplicantEizo Corporation
Decision Date2017-04-27
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RadiForce MX315W is a medical device manufactured by Eizo Corporation. It received FDA 510(k) clearance on 2017-04-27 under approval number K170949. 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 MX315W?
RadiForce MX315W is a medical device that received FDA 510(k) clearance on 2017-04-27. It is manufactured by Eizo Corporation. The 510(k) number is K170949.
When was RadiForce MX315W approved by the FDA?
RadiForce MX315W received FDA 510(k) clearance on 2017-04-27, under approval number K170949.
What company makes RadiForce MX315W?
RadiForce MX315W is manufactured by Eizo Corporation.
What is the FDA product code for RadiForce MX315W?
The FDA product code for RadiForce MX315W 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.