FDA 510(k) Applications Submitted by SOPHIE REHAULT
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150831 | 03/30/2015 | Cellvizio 100 Series System with Confocal Miniprobes | MAUNA KEA TECHNOLOGIES |
| K151593 | 06/12/2015 | Cellvizio 100 Series System with Confocal Miniprobes | MAUNA KEA TECHNOLOGIES |
| K162531 | 09/09/2016 | STERISPINE CC | SAFE ORTHOPAEDICS |
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