ClearanceBrief
510(k) K041018 ยท HHT Spatula, Cervical, Cytological

DRG SOFTRELEASE

ApplicantDoctor'S Research Group, Inc., Plymouth CT, US
DecisionSubstantially Equivalent, Oct 18, 2004
ReceivedApr 20, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041018

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.