510(k) K011710 ยท MYI System, Test, Genotypic Detection, Resistant Markers, Staphylococcus Colonies
OXOID PBP2 1 LATEX AGGLUTINATION TEST
| Applicant | Oxoid , Ltd., Basingstoke, GB |
| Decision | Substantially Equivalent, Apr 2, 2002 |
| Received | Jun 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011710
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.