Software Device To Aid In The Prediction Or Diagnosis Of Sepsis
General Hospital · 21 CFR 880.6316
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.
Recent MDR events
32 adverse event reports on file
- SEPSISJun 29, 2026MalfunctionCerner Corporation1931259-2026-00014
- SEPSISJun 24, 2026MalfunctionCerner Corporation1931259-2026-00012
- SEPSISJun 24, 2026MalfunctionCerner Corporation1931259-2026-00013
- SEPSISMay 22, 2026MalfunctionCerner Corporation1931259-2026-00009
- SEPSISMay 18, 2026MalfunctionCerner Corporation1931259-2026-00011
- SEPSISMay 6, 2026MalfunctionCerner Corporation1931259-2026-00010
- SEPSISApr 21, 2026MalfunctionCerner Corporation1931259-2026-00008
- SEPSISApr 3, 2026MalfunctionCerner Corporation1931259-2026-00007
- SEPSISMar 30, 2026MalfunctionCerner Corporation1931259-2026-00006
- SEPSISMar 26, 2026Malfunction1931259-2025-00008
Event type breakdown
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
1 firms currently registered for this product code
510(k) clearances
2 clearances for this product code