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510(k) Data Aggregation
K Number
K234141Device Name
AISAP Cardio V1.0
Manufacturer
Aisap
Date Cleared
2024-08-01
(216 days)
Product Code
POK, QIH
Regulation Number
892.2060Why did this record match?
Applicant Name (Manufacturer) :
Aisap
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
AISAP CARDIO V1.0 is a software platform that automatically processes and analyzes acquired cardiac POCUS images, producing a report with diagnostic assessment and measurements of several key cardiac structural and functional parameters, including: presence of valvular pathology (regurgitations of the mitral, tricuspid, aortic valves and aortic stenosis), and measurements of the Left Ventricle Ejection Fraction (LVEF), right and left ventricular dimensions, right ventricular fractional area change (RV FAC), atrial areas, ascending aorta diameter, and inferior vena cava (IVC) diameter.
The device outputs are provided in a report that is intended to support qualified physicians in their analysis and interpretation of adult cardiac POCUS images, using FDA-cleared ultrasound devices. Physicians should be trained and privileged by their organization following education processes and should perform cardiac POCUS according to their specialty professional society clinical guidelines.
AISAP CARDIO V1.0 has not been validated for the assessment of congenital heart disease, and/or intra-cardiac lesions (e.g., tumors, thrombi, vegetations), prosthetic valves, and in the presence of ventricular assist devices.
AISAP CARDIO V1.0 is indicated for use in adult patients only.
Device Description
AISAP CARDIO V1.0 is a machine learning-based decision support software device, indicated as an adjunct to diagnostic Cardiac point of care ultrasound (C-POCUS) for adult patients undergoing assessment for cardiac disease. This device performs automated analysis of ultrasound images and generates valvular assessments and measurements of standard cardiac structural and functional parameters.
- 1. Inform the user of a suspected cardiac valvular regurgitation (mitral, tricuspid, or aortic), and/or aortic stenosis is: either greater than mild severity or none to mild severity.
- 2. Inform the user of the 4 class American Society of Echocardiography (ASE) recommended category for valvular regurgitation (mitral, tricuspid, or aortic), and or aortic stenosis. Each finding categorizes according to none, mild, moderate, or severe.
- 3. Measurements of the following standard cardiac structural or functional parameters:
- Left Ventricular Ejection Fraction (LVEF) (percent) a.
- Left ventricular end diastolic diameter (cm) b.
- Right ventricular area change (RV FAC [ratio]) C.
- Inferior vena cava (IVC) maximal diameter (mm) d.
- e. Aortic root diameter (cm)
- ਿ Right atrium (RA) area (cm2)
- Left atrium (LA) area (cm²) g.
AISAP CARDIO V1.0 assists the physician in assessing 4 major valvular findings in adults, along with providing information on several correlated cardiac ultrasound measurements frequently found to be abnormal in association with valvular heart disease. Used together and interpreted by the physician, the device provides information that may assist in rendering an accurate diagnosis of selected cardiac findings. AISAP CARDIO V1.0 is adjunctive to cardiac POCUS (C-POCUS) use by privileged physicians in use scenarios supported by clinical guidelines. Specifically, patient management decisions are not intended to be and should not be made solely on the results of the software analysis of the proposed device. When significant valve pathology is suspected comprehensive echocardiography should be considered in accordance with the relevant professional guidelines.
AISAP CARDIO V1.0 uses machine learning NN (neural network) models trained to recognize patterns and make decisions. AISAP CARDIO V1.0 contains classification models which identify categories within data, regression models which predict numerical values, and instance segmentation models that detect and segment objects within images.
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