510(k) K890171 ยท CAC Apparatus, Autotransfusion
INLINE AUTOTRANSFUSION SYSTEM
| Applicant | Conmedcorp, Utica NY, US |
| Decision | Substantially Equivalent, Jun 15, 1989 |
| Received | Jan 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890171
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.