FDA 510(k) Applications Submitted by MARY ANN DU BROCK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030590 | 02/25/2003 | CLA ALLERGEN-SPECIFIC IGE ASSAY-LATEX ALLERGEN (K82) | HITACHI CHEMICAL DIAGNOSTICS, INC. |
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