510(k) K873299 ยท GWD Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp
MERIFLUOR(TM)-GIARDIA
| Applicant | Meridian Diagnostics, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Sep 16, 1987 |
| Received | Aug 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873299
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.