Last synced on 18 April 2025 at 11:05 pm

Software Device To Aid In The Prediction Or Diagnosis Of Sepsis

Page Type
Product Code
Definition
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.
Physical State
Software device
Technical Method
Use of algorithms to analyze clinical parameters to aid care providers with the prediction or diagnosis of sepsis.
Target Area
Software device for sepsis
Regulation Medical Specialty
General Hospital
Review Panel
Gastroenterology and Urology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6313
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SAK is linked to regulation 21CFR880.6313, which does not seem to exist yet. It may be pending at the moment.

Software Device To Aid In The Prediction Or Diagnosis Of Sepsis

Page Type
Product Code
Definition
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.
Physical State
Software device
Technical Method
Use of algorithms to analyze clinical parameters to aid care providers with the prediction or diagnosis of sepsis.
Target Area
Software device for sepsis
Regulation Medical Specialty
General Hospital
Review Panel
Gastroenterology and Urology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6313
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SAK is linked to regulation 21CFR880.6313, which does not seem to exist yet. It may be pending at the moment.