510(k) K934798 ยท LIN Antisera, Conjugated Fluorescent, Cytomegalovirus
PATHODX CYTOMEGALOVIRUS
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Mar 25, 1994 |
| Received | Oct 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934798
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.