510(k) K060929 ยท CDD Radioassay, Vitamin B12
IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6
| Applicant | Diagnostic Products Corporation, Los Angeles CA, US |
| Decision | Substantially Equivalent, Apr 28, 2006 |
| Received | Apr 5, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060929
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.