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FDA 510(k)

CX50N

K-Number: K222719 · 2023-05-09

Decision Date2023-05-09
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CX50N is the device name listed in this FDA 510(k) record. The listed applicant is Wide Corporation. It received FDA 510(k) clearance on 2023-05-09 under 510(k) 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. The listed applicant is Wide Corporation. The 510(k) number is K222719.

When did CX50N receive FDA 510(k) clearance?

CX50N received FDA 510(k) clearance on 2023-05-09, under 510(k) number K222719.

Who is the listed applicant for CX50N?

The FDA 510(k) record lists Wide Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CX50N?

The FDA product code for CX50N is PGY.

Other records listing Wide Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 14 devices →

Related Devices (Code: PGY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.