FDA 510(k) Applications Submitted by MEDAX S.R.L. UNIPERSONALE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172344 | 08/02/2017 | Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) | MEDAX S.R.L. UNIPERSONALE |
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