510(k) K883083 ยท GSA Antisera, All Mycoplasma Spp.
MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM
| Applicant | Medical Diagnostic Technologies, Inc., Augusta GA, US |
| Decision | Substantially Equivalent, Oct 25, 1988 |
| Received | Jul 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883083
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.