510(k) K093535 ยท CAC Apparatus, Autotransfusion
AUTOLOG AUTOTRANSFUSION SYSTEM
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 22, 2010 |
| Received | Nov 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093535
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.