510(k) K971897 ยท LFK Catheter, Femoral
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)
| Applicant | Medron, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 21, 1997 |
| Received | May 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971897
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.