ClearanceBrief
510(k) K182002 ยท MQL Media, Reproductive

Cumulus Remover

ApplicantKitazato Corporation, Shizuoka, JP
DecisionSubstantially Equivalent, Oct 23, 2018
ReceivedJul 26, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182002

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.