Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CW120N

K-Number: K210491 · 2021-04-08

ApplicantWide Corporation
Decision Date2021-04-08
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CW120N is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2021-04-08 under approval number K210491. 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 CW120N?

CW120N is a medical device that received FDA 510(k) clearance on 2021-04-08. It is manufactured by Wide Corporation. The 510(k) number is K210491.

When was CW120N approved by the FDA?

CW120N received FDA 510(k) clearance on 2021-04-08, under approval number K210491.

What company makes CW120N?

CW120N is manufactured by Wide Corporation.

What is the FDA product code for CW120N?

The FDA product code for CW120N is PGY.

Other Devices by Wide Corporation

K160354MX50T(MX50TQS) K160353MX50N(MX50YQS) K160348CX30N (CX30PQX) K160346MX30N(MX30TQS) K160355CX20N(CX20PUX) K160351CX50N, CX50YQS

View all 14 devices →

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.

↑