510(k) K901232 ยท CAC Apparatus, Autotransfusion
IMPRAFLO AUTOTRANSFUSION DEVICE
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Jul 18, 1990 |
| Received | Mar 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901232
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.