ClearanceBrief
510(k) K830785 ยท

LEECO DIG-QUANT DIAG. TEST KIT

ApplicantLeeco Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 8, 1983
ReceivedMar 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830785

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.