FDA 510(k) Applications Submitted by SYNERGENT BIOCHEM INC.-CLINICAL CONTROLS DIV.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010030 | 01/03/2001 | LIQUISPX HDL/LDL LIQUID CHOLESTEROL CALIBRATOR | SYNERGENT BIOCHEM INC.-CLINICAL CONTROLS DIV. |
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