Alere San Diego, Inc (Formally Biosite Incorporate is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alere San Diego, Inc (Formally Biosite Incorporate - FDA 510(k) Clear...
1
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Cleared
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Denied
Alere San Diego, Inc (Formally Biosite Incorporate has 0 FDA 510(k) cleared medical devices. Based in San Deigo, US.
Historical record: 0 cleared submissions from 2012 to 2012. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Alere San Diego, Inc (Formally Biosite Incorporate Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alere San Diego, Inc (Formally Biosite Incorporate
1 devices