Aerobiotix, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Aerobiotix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Miamisburg, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Aerobiotix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Aerobiotix, Inc.
1 devices