Infrascan, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Infrascan, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Infrascanner Model 2500 (Model 2500), Infrascanner, Infrascanner
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.
FDA 510(k) Regulatory Record - Infrascan, Inc.
5 devices