Annalise-Ai Pty , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Annalise-Ai Pty , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Annalise Enterprise CTB Triage Trauma, Annalise Enterprise CTB Triage Trauma, Annalise Enterprise CTB Triage-OH
6
Total
6
Cleared
0
Denied
Annalise-Ai Pty , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Sydney, AU.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Annalise-Ai Pty , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Annalise-Ai Pty , Ltd.
6 devices
Cleared
Sep 22, 2023
Annalise Enterprise CTB Triage Trauma
Radiology
133d
Cleared
Sep 22, 2023
Annalise Enterprise CTB Triage Trauma
Radiology
98d
Cleared
Aug 15, 2023
Annalise Enterprise CTB Triage-OH
Radiology
119d
Cleared
Apr 03, 2023
Annalise Enterprise CTB Triage Trauma
Radiology
165d
Cleared
Mar 28, 2023
Annalise Enterprise CXR Triage Trauma
Radiology
249d
Cleared
Mar 28, 2023
Annalise Enterprise CXR Triage Trauma
Radiology
243d