510(k) K833352 ยท GIL Plasma, Fibrinogen Control
GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROL
| Applicant | Warner-Lambert Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 3, 1983 |
| Received | Sep 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833352
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.