510(k) K852247 ยท DDB Ceruloplasmin, Antigen, Antiserum, Control
LASER CERULOPLASMIN KIT(CERULOPLASMIN REAGENTS)
| Applicant | Behring Diagnostics, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Jul 10, 1985 |
| Received | May 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852247
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.