510(k) K932074 ยท FIE Needle, Fistula
MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
| Applicant | Medisystems Corp., San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 18, 1994 |
| Received | Apr 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932074
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.