510(k) K830783 ยท JWX Kit, Screening, Staphylococcus Aureus
VERI-STAPH
| Applicant | Zeus Technologies, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 8, 1983 |
| Received | Mar 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830783
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.