510(k) K981084 ยท JXA Kit, Screening, Urine
URISCREEN
| Applicant | Diatech Diagnostics,Inc., Beverly MA, US |
| Decision | Substantially Equivalent, Oct 7, 1998 |
| Received | Mar 25, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981084
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.