510(k) K951821 ยท LIN Antisera, Conjugated Fluorescent, Cytomegalovirus
CYTOMEGALOVIRUS DIRECT IMMUNOFLUORESCENCE ASSAY
| Applicant | Light Diagnostics, Temecula CA, US |
| Decision | Substantially Equivalent, Jun 7, 1996 |
| Received | Apr 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951821
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.