510(k) K896777 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE
| Applicant | Research Medical, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 27, 1990 |
| Received | Dec 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896777
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.