510(k) K971619 ยท KRA Catheter, Continuous Flush
MICROFUSE MEMBRANE INFUSION CATHETER
| Applicant | E-Med Corp., Saint Paul MN, US |
| Decision | Substantially Equivalent, Feb 27, 1998 |
| Received | May 1, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971619
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.