FDA 510(k) Application Details - K231586

Device Classification Name	Computer, Blood-Pressure   More FDA Info for this Device
510(K) Number	K231586
Device Name	Computer, Blood-Pressure
Applicant	Endophys Technologies LLC 1933 E Levee St Suite B Dallas, TX 75207 US Other 510(k) Applications for this Company
Contact	Zachary Sowell Other 510(k) Applications for this Contact
Regulation Number	870.1110   More FDA Info for this Regulation Number
Classification Product Code	DSK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2023
Decision Date	11/03/2023
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