510(k) K770655 ยท GJP Control, Platelet
LATELET DETERMIBATION KIT, UL 800
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Jun 24, 1977 |
| Received | Apr 6, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770655
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.