Corvair
K-Number: K231010 · 2024-06-07
ApplicantAliveCor, Inc.
Decision Date2024-06-07
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Corvair is a medical device manufactured by AliveCor, Inc.. It received FDA 510(k) clearance on 2024-06-07 under approval number K231010. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Corvair?
Corvair is a medical device that received FDA 510(k) clearance on 2024-06-07. It is manufactured by AliveCor, Inc.. The 510(k) number is K231010.
When was Corvair approved by the FDA?
Corvair received FDA 510(k) clearance on 2024-06-07, under approval number K231010.
What company makes Corvair?
Corvair is manufactured by AliveCor, Inc..
What is the FDA product code for Corvair?
The FDA product code for Corvair is MHX.
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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.