510(k) K952251 ยท JJX Single (Specified) Analyte Controls (Assayed And Unassayed)
IMMULITE HCG HIGH LEVEL CONTROL MODULE
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Sep 8, 1995 |
| Received | May 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952251
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.