510(k) K894805 ยท JXA Kit, Screening, Urine
RAPIDEC UR
| Applicant | Dms Products, Inc., Flemington NJ, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Jul 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894805
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.