Pressio, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pressio, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pressio, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Pressio, Inc.
1 devices