510(k) K882767 ยท GKH Apparatus, Automated Blood Cell Diluting
SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM
| Applicant | Toa Medical Electronics USA, Inc., Los Alamitos CA, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | Jul 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882767
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.