Respiri Limited is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Respiri Limited - FDA 510(k) Cleared Devices
Recent clearances: wheezo WheezeRate Detector
1
Total
1
Cleared
0
Denied
Respiri Limited has 1 FDA 510(k) cleared medical devices. Based in Melbourne, AU.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Respiri Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Respiri Limited
1 devices