510(k) K812621 ยท FIE Needle, Fistula
DELTA-A.V. FISTULA CANNULATION SET
| Applicant | Amisco Trading Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 24, 1981 |
| Received | Sep 15, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812621
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.