ClearanceBrief
510(k) K875219 ยท LDJ Enzyme Immunoassay, Cannabinoids

MODIFICATION TO KDI QUIK TEST MARIJUANA SCREEN

ApplicantKeystone Diagnostics, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jun 24, 1988
ReceivedDec 22, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875219

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.