St. Jude Medical Systems AB
FDA 510(k) & PMA Approved Devices — 4 products
Advertisement
Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K133587 | PRESSUREWIRE AERIS AGILE TIP; PRESSUREWIRE AERIS AGILE TIP 300 | DRG | 2013-12-20 | View |
| 510(k) | K131452 | PRESSUREWIRE; CERTUS, CERTUS 300, AERIS, AERIS 300 | DXO | 2013-09-05 | View |
| 510(k) | K111854 | AO USB RECEIVER, WI-BOX, WI-BOX PSU KIT, WI-BOX XPRESS CABLE, PW USB RECEIVER | DRG | 2011-10-21 | View |
| 510(k) | K110193 | FEMOSTOP PLYS, FEMOSTOP HD, FEMOSTOP COMPRESSION ARCH; FEMOSTOP II PLUS SET; FEMOSTOP II PLUS ARCH, BILATERAL ADAPTER; F | DXC | 2011-02-24 | View |
No matching devices.
Advertisement