FDA 510(k) Applications Submitted by ROCHE PROFESSIONAL DIAGNOSTICS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100903 | 04/01/2010 | ANTI-HAV | ROCHE PROFESSIONAL DIAGNOSTICS |
| K143534 | 12/12/2014 | Elecsys CA-125 II assay | ROCHE PROFESSIONAL DIAGNOSTICS |
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