510(k) K811412 ยท JSX Kit, Identification, Neisseria Gonorrhoeae
NEISSERIA-KWIK
| Applicant | Windsor Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 16, 1981 |
| Received | May 19, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811412
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.