SIF
- 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.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN250057 | 2026-05-22 | Cardiosense, Inc. | PCWP Analysis Software | — |
Official FDA classification page: SIF
Classification and pathway per current FDA publications. Data from openFDA (CC0).