510(k) K850409 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
GEN. DIAG. CHROMOSTRATE REF. PLASMA
| Applicant | Warner-Lambert Co., Morris Plains NJ, US |
| Decision | Substantially Equivalent, May 8, 1985 |
| Received | Feb 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850409
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.