CORDIS PERMANENT PERVENOUS CARDIAC LEADS — Cordis Corp. (510(k) K791768)
CORDIS PERMANENT PERVENOUS CARDIAC LEADS — Cordis Corp. (510(k) K791768) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: CORDIS PERMANENT PERVENOUS CARDIAC LEADS; Applicant: Cordis Corp.; Clearance track: 510(k).
| Device name | CORDIS PERMANENT PERVENOUS CARDIAC LEADS |
|---|---|
| Applicant | Cordis Corp. |
| Clearance track | 510(k) |
| Submission number | K791768 |
| Decision | Substantially Equivalent |
| Decision date | 1979-11-05 |
| Date received | 1979-09-05 |
| Product code | DTB |
| Device class | 3 |
| Medical specialty | Cardiovascular |
| Applicant location | MI, US |
| Source | openFDA device |
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$1999/mo
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