510(k) K041743 ยท DKZ Enzyme Immunoassay, Amphetamine
ACON TRI-FECT DRUG SCREEN TEST DEVICE
| Applicant | ACON Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 9, 2004 |
| Received | Jun 28, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041743
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.