510(k) K961927 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
RMI HEMOCONCENTRACTOR TUBING SET
| Applicant | Research Medical, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Aug 13, 1996 |
| Received | May 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961927
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.