510(k) K926409 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic
PLASMA DISCARD BAGS
| Applicant | Apheresis Technologies, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 2, 1993 |
| Received | Dec 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926409
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.