510(k) K994171 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE
| Applicant | Medtronic Cardiac Surgical Products, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Apr 27, 2000 |
| Received | Dec 10, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994171
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.