Oxavita Srl is one of 7 FDA 510(k) medical device manufacturers from Argentina in the dataset, ranked by real submission volume.
Oxavita Srl - FDA 510(k) Cleared Devices
Recent clearances: Revitalair 430F
1
Total
1
Cleared
0
Denied
Oxavita Srl has 1 FDA 510(k) cleared medical devices. Based in Buenos Aires, AR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Oxavita Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Oxavita Srl
1 devices