SIF

Software Device System For Estimation Of Cardiac Pressures

Product code
SIF
Device name
Software Device System For Estimation Of Cardiac Pressures
Device class
Class 2
21 CFR
21 CFR 870.1150
Medical specialty
Cardiovascular
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
0 (direct download)
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)

FDA classification definition

This prescription-only device uses machine learning-based algorithms to analyze one or more non-invasive physiologic signals or parameters to estimate a cardiac pressure (e.g. pulmonary capillary wedge pressure, left ventricular end diastolic pressure, or pulmonary artery pressure.) This device is intended for adjunctive use with patient information and is not intended to independently direct therapy. The device may contain hardware sensors. This device is not intended to estimate systemic, vascular blood pressure.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2026-05-22.

NumberDecision dateApplicantDevice nameSummary
DEN2500572026-05-22Cardiosense, Inc.PCWP Analysis Software
Official FDA classification page: SIF
Classification and pathway per current FDA publications. Data from openFDA (CC0).