ClearanceBrief
510(k) K032836 ยท HNO Keratome, Ac-Powered

M3 MICROKERATOME

ApplicantMoria SA, Antony, FR
DecisionSubstantially Equivalent, Jun 18, 2004
ReceivedSep 11, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032836

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.