Pression, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pression, Inc. has 1 FDA 510(k) cleared medical devices. Based in Coatesville, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pression, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Broderick Regulatory Consulting, LLC as regulatory consultant.
1 devices