510(k) K893962 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic
COBE 2991 SUPPLEMENTARY DISPOSABLE SETS
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Oct 18, 1989 |
| Received | Jun 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893962
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.