FDA 510(k) Applications Submitted by MEDICON HELLAS S.A.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062746 | 09/14/2006 | FERRITIN-LATEX, MODELS 1418-2070, 1418-0279 | MEDICON HELLAS S.A. |
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