510(k) K000753 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORDIS 13F CATHETER SHEATH INTRODUCER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 6, 2000 |
| Received | Mar 8, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000753
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.