Neumodx Molecular, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Neumodx Molecular, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Last cleared in 2023. Active since 2018. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Neumodx Molecular, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qiagen as regulatory consultant.
2 devices