Embol-X, 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) | K022071 | EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000 | DTM | 2003-02-14 | View |
| 510(k) | K020693 | AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100; AORTIC CANNULA, PLASTIC J-TIP (24FR) MODEL #CF00101 | DWF | 2002-09-05 | View |
| 510(k) | K002973 | EMBOL-X INTRODUCER, MODEL CF00200 | DYB | 2001-04-26 | View |
| 510(k) | K980631 | EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA | DXC | 1999-02-02 | View |
No matching devices.
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