510(k) K905617 ยท JWX Kit, Screening, Staphylococcus Aureus
VISI-STAPH
| Applicant | Connecticut Diagnostics, Ltd., Danielson CT, US |
| Decision | Substantially Equivalent, Mar 29, 1991 |
| Received | Dec 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905617
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.