510(k) K162423 ยท CAC Apparatus, Autotransfusion
Haemonetics Cell Saver Elite/Elite+ Autotransfusion System
| Applicant | Haemonetics Corporation, Braintree MA, US |
| Decision | Substantially Equivalent, Jan 3, 2017 |
| Received | Aug 30, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162423
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.