Banyan USA, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Banyan USA, LLC has 1 FDA 510(k) cleared medical devices. Based in Hauppauge, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Banyan USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
1 devices