CX50N
K-Number: K222719 · 2023-05-09
ApplicantWide Corporation
Decision Date2023-05-09
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CX50N is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2023-05-09 under approval number K222719. 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 CX50N?
CX50N is a medical device that received FDA 510(k) clearance on 2023-05-09. It is manufactured by Wide Corporation. The 510(k) number is K222719.
When was CX50N approved by the FDA?
CX50N received FDA 510(k) clearance on 2023-05-09, under approval number K222719.
What company makes CX50N?
CX50N is manufactured by Wide Corporation.
What is the FDA product code for CX50N?
The FDA product code for CX50N 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.