510(k) K850682 ยท DDB Ceruloplasmin, Antigen, Antiserum, Control
72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL
| Applicant | Kent Laboratories, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Nov 25, 1985 |
| Received | Feb 21, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850682
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.