FDA 510(k) Applications Submitted by ALERE, SAN DIEGO, DBA BIOSITE INCORPORATED, DBA IN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102700 | 09/20/2010 | LIPID CONTROLS; MULTI- ANALYTE CONTROL; MULTI-ANALYTE CALIBRATION VERIFICATION MATERIALS | ALERE, SAN DIEGO, DBA BIOSITE INCORPORATED, DBA IN |
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