FDA 510(k) Applications Submitted by TYRX , INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132699 | 08/29/2013 | AIGIS RX N (MEDIUM), AIGIS RX N (LARGE) | TYRX , INC. |
| K130943 | 04/04/2013 | AIGIS RX R PM/ AIGIS RX R ICD | TYRX , INC. |
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