FDA 510(k) Application Details - K203224

Device Classification Name	More FDA Info for this Device
510(K) Number	K203224
Device Name	Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform
Applicant	Edwards Lifesciences, LLC One Edwards Way Irvine, CA 92614 US Other 510(k) Applications for this Company
Contact	Lisa Gilman Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QAQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/02/2020
Decision Date	07/30/2021
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