510(k) K875367 ยท GQM Antisera, Neutralization, Herpesvirus Hominis
COLORGENE FLUORESCENT DNA HYBRIDIZATION TEST / CMV
| Applicant | Enzo Biochem, Inc., New York NY, US |
| Decision | Substantially Equivalent, Mar 28, 1988 |
| Received | Dec 31, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875367
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.