510(k) K900105 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic
COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Mar 22, 1991 |
| Received | Jan 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900105
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.