510(k) K861716 ยท GRZ Antisera, Fluorescent, All, Mycoplasma Spp.
FIAX TEST KIT FOR MYCOPLASMA PNEUMONIAE-G ANTIBODY
| Applicant | Whittaker Bioproducts, Inc., Walkersville MD, US |
| Decision | Substantially Equivalent, Aug 8, 1986 |
| Received | May 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861716
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.