510(k) K882211 ยท JXA Kit, Screening, Urine
URISCREEN
| Applicant | Diatech Diagnostica , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Sep 30, 1988 |
| Received | May 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882211
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.