CX50N, CX50YQS
K-Number: K160351 · 2016-04-07
ApplicantWide Corporation
Decision Date2016-04-07
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CX50N, CX50YQS is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2016-04-07 under approval number K160351. 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, CX50YQS?
CX50N, CX50YQS 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 K160351.
When was CX50N, CX50YQS approved by the FDA?
CX50N, CX50YQS received FDA 510(k) clearance on 2016-04-07, under approval number K160351.
What company makes CX50N, CX50YQS?
CX50N, CX50YQS is manufactured by Wide Corporation.
What is the FDA product code for CX50N, CX50YQS?
The FDA product code for CX50N, CX50YQS is PGY.
Other Devices by Wide Corporation
Related Devices (Code: PGY)
K1633356MP Color LCD Monitor, RadiForce RX660, RX660-AREizo Corporation
K1625278MP Color LCD Monitor (C81W+)Shenzhen Beacon Display Technology Co., Ltd.
K1624975MP Monochrome LCD Monitor, RadiForce GX550, GX550-AREizo Corporation
K1618952MP Color LCD Monitor CCL214 (CL21214)Jvckenwood Corporation
K162196Dell UP3216Q with QUBYX PerfectLum bundleQubyx Software Technologies, Inc.
K161229Mammo Tomosynthesis (MDMG-5221)Barco N.V.
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.