510(k) K820895 ยท LIN Antisera, Conjugated Fluorescent, Cytomegalovirus
CYLOMEGALOVIRUS DIRECT FLUORESCENT ANTI
| Applicant | Bartels Immunodiagnostic Supplies, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 3, 1982 |
| Received | Mar 30, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820895
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.