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)

CW60N

K-Number: K222722 · 2022-10-31

Decision Date2022-10-31
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CW60N is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2022-10-31 under approval number K222722. 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 CW60N?

CW60N is a medical device that received FDA 510(k) clearance on 2022-10-31. It is manufactured by Wide Corporation. The 510(k) number is K222722.

When was CW60N approved by the FDA?

CW60N received FDA 510(k) clearance on 2022-10-31, under approval number K222722.

What company makes CW60N?

CW60N is manufactured by Wide Corporation.

What is the FDA product code for CW60N?

The FDA product code for CW60N is PGY.

Other Devices by Wide Corporation

View all 14 devices →

Related Devices (Code: PGY)

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.