MSKai
K-Number: K240793 · 2024-12-16
ApplicantMskai
Decision Date2024-12-16
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MSKai is the device name listed in this FDA 510(k) record. The listed applicant is Mskai. It received FDA 510(k) clearance on 2024-12-16 under 510(k) number K240793. 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 MSKai?
MSKai is a medical device that received FDA 510(k) clearance on 2024-12-16. The listed applicant is Mskai. The 510(k) number is K240793.
When did MSKai receive FDA 510(k) clearance?
MSKai received FDA 510(k) clearance on 2024-12-16, under 510(k) number K240793.
Who is the listed applicant for MSKai?
The FDA 510(k) record lists Mskai as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MSKai?
The FDA product code for MSKai is QIH.
Related Devices (Code: QIH)
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
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