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FDA 510(k)

Corsano CardioWatch 287-2 System

K-Number: K232548 · 2024-03-22

ApplicantCorsano Health B.V.
Decision Date2024-03-22
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Corsano CardioWatch 287-2 System is a medical device manufactured by Corsano Health B.V.. It received FDA 510(k) clearance on 2024-03-22 under approval number K232548. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Corsano CardioWatch 287-2 System?

Corsano CardioWatch 287-2 System is a medical device that received FDA 510(k) clearance on 2024-03-22. It is manufactured by Corsano Health B.V.. The 510(k) number is K232548.

When was Corsano CardioWatch 287-2 System approved by the FDA?

Corsano CardioWatch 287-2 System received FDA 510(k) clearance on 2024-03-22, under approval number K232548.

What company makes Corsano CardioWatch 287-2 System?

Corsano CardioWatch 287-2 System is manufactured by Corsano Health B.V..

What is the FDA product code for Corsano CardioWatch 287-2 System?

The FDA product code for Corsano CardioWatch 287-2 System is MSX.

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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.

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