510(k) K871831 ยท GTZ Antisera, All Groups, Streptococcus Spp.
PATHO DX LATEX AGGLUTINATION STREP GROUPING KIT
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jun 17, 1987 |
| Received | May 11, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871831
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.