Telectronics and Cordis Pacing Systems
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K883265 | MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD | DTB | 1988-10-14 | View |
| 510(k) | K881904 | CHANGE TO CATHODE POWDER SPECIFICATION | DXY | 1988-07-22 | View |
| 510(k) | K881711 | VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA. | DXY | 1988-05-26 | View |
No matching devices.
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