CX20N(CX20PUX)
K-Number: K160355 · 2016-04-07
ApplicantWide Corporation
Decision Date2016-04-07
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CX20N(CX20PUX) is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2016-04-07 under approval number K160355. 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 CX20N(CX20PUX)?
CX20N(CX20PUX) is a medical device that received FDA 510(k) clearance on 2016-04-07. It is manufactured by Wide Corporation. The 510(k) number is K160355.
When was CX20N(CX20PUX) approved by the FDA?
CX20N(CX20PUX) received FDA 510(k) clearance on 2016-04-07, under approval number K160355.
What company makes CX20N(CX20PUX)?
CX20N(CX20PUX) is manufactured by Wide Corporation.
What is the FDA product code for CX20N(CX20PUX)?
The FDA product code for CX20N(CX20PUX) 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.