510(k) K801966 ยท FIE Needle, Fistula
HEMO-CATH II KIDNEY DIALYSIS CATHETER
| Applicant | Medical Components, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1980 |
| Received | Aug 19, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801966
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.