510(k) K894002 ยท LIN Antisera, Conjugated Fluorescent, Cytomegalovirus
CYTOMEGALOVIRUS FLUORESCENT MONOCLONAL ANTIBODY
| Applicant | Baxter Healthcare Corp, Bellevue WA, US |
| Decision | Substantially Equivalent, Aug 10, 1989 |
| Received | Jun 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894002
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.