FDA 510(k) Applications Submitted by DENKA SEIKEN'S
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011400 | 05/07/2001 | MRSA-SCREEN | DENKA SEIKEN'S |
| K981734 | 05/18/1998 | VTEC-RPLA SEIKEN | DENKA SEIKEN'S |
| K011958 | 06/22/2001 | CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT | DENKA SEIKEN'S |
| K013359 | 10/10/2001 | LP(A)-LATEX SEIKEN ASSAY KIT | DENKA SEIKEN'S |
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