510(k) K890717 ยท LFK Catheter, Femoral
MODIFICATION HEMOFILTRATION CATHETER HF-100
| Applicant | Vas-Cath, Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Apr 5, 1989 |
| Received | Feb 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890717
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.