Mesa Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mesa Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Accula Strep A Test, Accula RSV Test, Accula Flu A/Flu B Test
3
Total
3
Cleared
0
Denied
Mesa Biotech, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 2018 to 2020. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Mesa Biotech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mesa Biotech, Inc.
3 devices