ClearanceBrief
510(k) K043183 ยท HNO Keratome, Ac-Powered

EPI-K

ApplicantMoria SA, Antony, FR
DecisionSubstantially Equivalent, Mar 25, 2005
ReceivedNov 17, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043183

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.