FDA 510(k) Applications Submitted by SWEDEN DIAGNOSTICS (US), INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061165 | 04/26/2006 | ELIA CCP, MODEL 14-5515-01; ELIA CCP CONTROL, MODEL 83-1009-01 | SWEDEN DIAGNOSTICS (US), INC. |
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