510(k) K860279 ยท LIN Antisera, Conjugated Fluorescent, Cytomegalovirus
CYTOMEGALOVIRUS DIRECT FLUORESCENT ANTIBODY KIT
| Applicant | Bartels Immunodiagnostic Supplies, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, May 13, 1986 |
| Received | Jan 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860279
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.