ClearanceBrief
510(k) K981155 ยท HNO Keratome, Ac-Powered

FLAPMAKER DISPOSABLE MICROKERATOME

ApplicantHawken Industries, Cleveland OH, US
DecisionSubstantially Equivalent, Aug 14, 1998
ReceivedMar 31, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981155

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.