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FDA 510(k) Application Details - K232294
Device Classification Name
Computer, Diagnostic, Programmable
More FDA Info for this Device
510(K) Number
K232294
Device Name
Computer, Diagnostic, Programmable
Applicant
Edwards Lifesciences, LLC
One Edwards Way
Irvine, CA 92614 US
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Contact
Varad Raghuwanshi
Other 510(k) Applications for this Contact
Regulation Number
870.1425
More FDA Info for this Regulation Number
Classification Product Code
DQK
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More FDA Info for this Product Code
Date Received
08/01/2023
Decision Date
10/31/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K232294
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