FDA 510(k) Applications Submitted by ROCHE DIAGNOSTICS OPERATIONS INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131029 | 04/12/2013 | ACCU-CHEK AVIVA PLUS TEST STRIP | ROCHE DIAGNOSTICS OPERATIONS INC |
| K131366 | 05/13/2013 | ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM | ROCHE DIAGNOSTICS OPERATIONS INC |
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