510(k) K900939 ยท KQJ System, Fibrinogen Determination
SPQ TEST SYSTEM II FOR FIB (SERUM PROTEIN QUANTI.)
| Applicant | Incstar Corp., Stillwater MN, US |
| Decision | Substantially Equivalent, May 16, 1990 |
| Received | Feb 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900939
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.