Tyrx, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K132699 | AIGIS RX N (MEDIUM), AIGIS RX N (LARGE) | FTL | 2013-11-26 | View |
| 510(k) | K131007 | AIGIS RX N MEDIUM; AIGIS RX N LARGE | FTL | 2013-07-10 | View |
| 510(k) | K130943 | AIGIS RX R PM/ AIGIS RX R ICD | FTL | 2013-05-20 | View |
| 510(k) | K093524 | PIVIT A/B ST AND PIVIT A/B ST-R | FTL | 2010-03-26 | View |
No matching devices.
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