510(k) K880218 ยท CFT Radioimmunoassay, Prolactin (Lactogen)
BINAX PROLACTIN IRMA DIAGNOSTIC KIT
| Applicant | Binax, Inc., S. Portland ME, US |
| Decision | Substantially Equivalent, Mar 1, 1988 |
| Received | Jan 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880218
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.