ClearanceBrief
510(k) K033236 ยท HNO Keratome, Ac-Powered

PRIZM KERATOME BLADE, MODEL MK8512M2

ApplicantSurgin Surgical Instrumentation, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Mar 26, 2004
ReceivedOct 6, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033236

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.