Infrascan, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
1
Denied
Infrascan, Inc. has 4 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Latest FDA clearance: Dec 2024. Active since 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Infrascan, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
5 devices