Alere, San Diego, Dba Biosite INcorporated, Dba IN is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alere, San Diego, Dba Biosite INcorporated, Dba IN - FDA 510(k) Clear...
1
Total
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Cleared
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Denied
Alere, San Diego, Dba Biosite INcorporated, Dba IN has 1 FDA 510(k) cleared medical devices. Based in San Deigo, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Alere, San Diego, Dba Biosite INcorporated, Dba IN Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alere, San Diego, Dba Biosite INcorporated, Dba IN
1 devices