510(k) K870117 ยท JSX Kit, Identification, Neisseria Gonorrhoeae
NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST
| Applicant | Pro-Lab, Inc., Scarborough Ont, CA |
| Decision | Substantially Equivalent, Mar 20, 1987 |
| Received | Jan 12, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870117
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.