Nucleix , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Nucleix , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Rehovot, IL.
Last cleared in 2023. Active since 2023. Primary specialty: Medical Genetics.
Browse the FDA 510(k) cleared devices submitted by Nucleix , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Nucleix , Ltd.
1 devices