510(k) K012143 ยท DRA Catheter, Steerable
24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524
| Applicant | Medtronic Cardiac Surgical Products, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Oct 24, 2001 |
| Received | Jul 10, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012143
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.