510(k) K882045 ยท LDF Electrode, Pacemaker, Temporary
HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK
| Applicant | Cordis Leads, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jul 12, 1988 |
| Received | May 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882045
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.