Cordis Leads, 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) | K883070 | ENCOR UNIPOLAR VS-1 LEADS | DTB | 1988-12-05 | View |
| 510(k) | K873772 | CHANGES TO ENCOR PERVENOUS J-ATRIAL LEADS | DTB | 1988-10-19 | View |
| 510(k) | K882045 | HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK | LDF | 1988-07-12 | View |
| 510(k) | K874366 | ENCOR BIPOLAR ACT/FIXA LEAD W/POR SUR ELE #329-201 | DTB | 1988-06-16 | View |
No matching devices.
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