FDA 510(k) Applications Submitted by BARBARA PREISEL-SIMMONS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K012183 | 07/12/2001 | BAYER DIAGNOSTICS ADVIA CENTAUR TOXOPLASMA IGG ASSAY | BAYER DIAGNOSTICS CORP. |
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