Anoxia Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anoxia Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Quiver Aspiration Pump, Slinky Catheter
2
Total
2
Cleared
0
Denied
Anoxia Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Hayward, US.
Latest FDA clearance: Feb 2024. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Anoxia Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Anoxia Medical, Inc.
2 devices