FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

Annalise Enterprise CTB Triage Trauma

K Number: K223240 · Decision Apr 3, 2023
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
85
Applicant Total
6
Review Days
165

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Basic Information

Device Name
Annalise Enterprise CTB Triage Trauma
K Number
K223240
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2080
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Annalise-Ai Pty , Ltd.
Date Received
October 20, 2022
Decision Date
April 3, 2023
Product Code
QAS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QAS Radiological Computer-Assisted Triage And Notification Software

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QAS), ordered by most recent decision date.

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Other Clearances by Annalise-Ai Pty , Ltd.

K Number Device Name
K231767 Annalise Enterprise CTB Triage Trauma
K231384 Annalise Enterprise CTB Triage Trauma
K231094 Annalise Enterprise CTB Triage-OH
K222268 Annalise Enterprise CXR Triage Trauma
K222179 Annalise Enterprise CXR Triage Trauma