ClearanceBrief
510(k) K993225 ยท HNO Keratome, Ac-Powered

BLADEWORKS MICROKERATOME BLADE

ApplicantBlade Works, Inc., Hillsboro TX, US
DecisionSubstantially Equivalent, Mar 20, 2000
ReceivedSep 27, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993225

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.