FDA 510(k)

MSK Go

K-Number: K260234 · 2026-05-21

ApplicantSmart Alfa Teknoloji San. Ve Tic. A.S.

Decision Date2026-05-21

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MSK Go is the device name listed in this FDA 510(k) record. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. It received FDA 510(k) clearance on 2026-05-21 under 510(k) number K260234. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSK Go?

MSK Go is a medical device that received FDA 510(k) clearance on 2026-05-21. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. The 510(k) number is K260234.

When did MSK Go receive FDA 510(k) clearance?

MSK Go received FDA 510(k) clearance on 2026-05-21, under 510(k) number K260234.

Who is the listed applicant for MSK Go?

The FDA 510(k) record lists Smart Alfa Teknoloji San. Ve Tic. A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSK Go?

The FDA product code for MSK Go is QIH.

Other records listing Smart Alfa Teknoloji San. Ve Tic. A.S. 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.