510(k) K895435 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic
FRESENIUS AS 104 CELL SEPARATOR
| Applicant | Fresenius USA, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Nov 2, 1990 |
| Received | Sep 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895435
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.