CL24N
K-Number: K222717 · 2022-10-31
Device Summary
Frequently Asked Questions
What is the CL24N?
CL24N is a medical device that received FDA 510(k) clearance on 2022-10-31. The listed applicant is Wide Corporation. The 510(k) number is K222717.
When did CL24N receive FDA 510(k) clearance?
CL24N received FDA 510(k) clearance on 2022-10-31, under 510(k) number K222717.
Who is the listed applicant for CL24N?
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 CL24N?
The FDA product code for CL24N 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.
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.