FDA 510(k), K232053, SimpleSense-BP, SimpleSense-BP Software Application

510(K) Number: K232053
Device Name: SimpleSense-BP, SimpleSense-BP Software Application
Manufacturer: Venkatesh Varadan
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Classification Product Code:  DXN
Date Received: 07/11/2023
Decision Date: 12/08/2023
Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular