Other

Sepsis ImmunoScore

Prenosis, Inc.

FDA-cleared AI medical device

A software device to aid in the prediction or diagnosis of sepsis uses advanced algorithms to analyze patient specific data to aid health care providers in the prediction and/or diagnosis of sepsis. The device is intended for adjunctive use and is not intended to be used as the sole determining factor in assessing a patient's sepsis status. The device may contain alarms that alert the care provider of the patient's status. The device is not intended to monitor response to treatment in patients being treated for sepsis.

FDA Submission Metadata

Submission number
DEN230036
Decision date
April 2024
FDA panel
General Hospital
Product code
SAK
Clinical task (npj)
predictive
Data modality (npj)
EHR

This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.

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