510(k) K192368 ยท CAC Apparatus, Autotransfusion
CATSmart
| Applicant | Fresenius Kabi AG, Bad Homburg, DE |
| Decision | Substantially Equivalent, Sep 27, 2019 |
| Received | Aug 30, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192368
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.