510(k) K913456 ยท JSX Kit, Identification, Neisseria Gonorrhoeae
VISI-NEISSERIA
| Applicant | Kev Connecticut Diagnostics, Inc., Danielson CT, US |
| Decision | Substantially Equivalent, Oct 11, 1991 |
| Received | Aug 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913456
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.