FDA 510(k) Applications Submitted by Roberto Gabriotti
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180293 | 02/01/2018 | Retia 2 | CenterVue SpA |
| K150320 | 02/09/2015 | COMPASS | CENTERVUE SPA |
| K180526 | 02/27/2018 | EIDON FA | CenterVue SpA |
| K192113 | 08/05/2019 | DRSplus | CenterVue SpA |
| K153181 | 11/03/2015 | MAIA | CENTERVUE SPA |
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