Seegene is one of 26017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seegene - FDA 510(k) Cleared Devices
Recent clearances: SEEGENE ANYPLEX II HSV-1/2 ASSAY
1
Total
1
Cleared
0
Denied
Seegene has 1 FDA 510(k) cleared medical devices. Based in Beverly, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Seegene Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MDC Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Seegene
1 devices