510(k) K862002 ยท FIE Needle, Fistula
MEDISYSTEMS PHERESIS NEEDLE
| Applicant | Medisystems Corp., Washington DC, US |
| Decision | Substantially Equivalent, Jun 27, 1986 |
| Received | May 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862002
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.