FDA 510(k) Applications Submitted by Therese CANDAU
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160730 | 03/16/2016 | Instrument kits | ANTHOGYR |
| K131066 | 04/16/2013 | AXIOM REG | ANTHOGYR SAS |
| K161177 | 04/26/2016 | Axiom PX | ANTHOGYR SAS |
| K141450 | 06/02/2014 | AXIOM 2.8 | ANTHOGYR SAS |
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