510(k) K892819 ยท CAC Apparatus, Autotransfusion
AUTOTRANSFUSION DEVICE
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, May 22, 1989 |
| Received | Apr 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892819
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.