510(k) K792718 ยท GMK Antiserum, Positive Control, Histoplasma Capsulatum
HISTOPLASMA CAPSULATUM, ANTISERUM
| Applicant | Meridian Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1980 |
| Received | Dec 27, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792718
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.