Anoxia Medical, Inc. - FDA 510(k) Cleared Devices
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: General & Plastic Surgery.
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.
2 devices