510(k) K842383 ยท GTZ Antisera, All Groups, Streptococcus Spp.
PATHO DX LATEX AGGLUTINATION STREP A
| Applicant | Diagnostic Products Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 2, 1984 |
| Received | Jun 18, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842383
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.