510(k) K141019 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic
AMICUS SEPARATOR SYSTEM/ AMICUS SEPERATOR SYSTEM;REFURBISHED
| Applicant | Fenwal, Inc., Lake Zurich IL, US |
| Decision | Substantially Equivalent, Jun 10, 2014 |
| Received | Apr 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141019
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.