ClearanceBrief
510(k) K941110 ยท LKS Device, Parasite Concentration

PARAKIT

ApplicantHardy Diagnostics, Santa Maria CA, US
DecisionSubstantially Equivalent, May 17, 1994
ReceivedMar 7, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941110

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.