ClearanceBrief
510(k) K994015 ยท HNO Keratome, Ac-Powered

ACCUBLADE (ACS MODEL), MK8507, ACCUBLADE (HANSOTOME MODEL), MK8508

ApplicantSurgin Surgical Instrumentation, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Mar 15, 2000
ReceivedNov 26, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K994015

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.