510(k) K845046 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
PUL,MONARY ARTERY VENT CATHETER
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Apr 3, 1985 |
| Received | Dec 28, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K845046
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.