MX50N(MX50YQS)
K-Number: K160353 · 2016-04-22
Device Summary
Frequently Asked Questions
What is the MX50N(MX50YQS)?
MX50N(MX50YQS) is a medical device that received FDA 510(k) clearance on 2016-04-22. The listed applicant is Wide Corporation. The 510(k) number is K160353.
When did MX50N(MX50YQS) receive FDA 510(k) clearance?
MX50N(MX50YQS) received FDA 510(k) clearance on 2016-04-22, under 510(k) number K160353.
Who is the listed applicant for MX50N(MX50YQS)?
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 MX50N(MX50YQS)?
The FDA product code for MX50N(MX50YQS) 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.