Mawi Dna Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mawi Dna Technologies - FDA 510(k) Cleared Devices
Recent clearances: iSWAB-Respiratory Tract Sample Collection Media-Extraction Less (iSWAB-RC-EL)
1
Total
1
Cleared
0
Denied
Mawi Dna Technologies has 1 FDA 510(k) cleared medical devices. Based in Hayward, US.
Last cleared in 2023. Active since 2023. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Mawi Dna Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mawi Dna Technologies
1 devices