Alere San Diego, Incorporated is one of 5033 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alere San Diego, Incorporated - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Alere San Diego, Incorporated has 1 FDA 510(k) cleared medical devices. Based in San Deigo, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Alere San Diego, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alere San Diego, Incorporated
1 devices