FDA 510(k) Applications Submitted by ARRINEX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160669 | 03/09/2016 | ClariFix Device | ARRINEX, INC. |
| K162608 | 09/19/2016 | ClariFix Device | ARRINEX, INC. |
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