Airphysio Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Airphysio Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AirPhysio Positive Expiratory Pressure (PEP) Device
1
Total
1
Cleared
0
Denied
Airphysio Pty, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Tweed Heads South, AU.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Airphysio Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Airphysio Pty, Ltd.
1 devices