Magbio Genomics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Magbio Genomics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MagXtract Collection Tube
1
Total
1
Cleared
0
Denied
Magbio Genomics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.
Last cleared in 2022. Active since 2022. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Magbio Genomics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Brij Strategic Consultations, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Magbio Genomics, Inc.
1 devices