ClearanceBrief
510(k) K013969 ยท KOJ Airbrush

MINIBLASTER

ApplicantDeldent , Ltd., Petach Tikvah, IL
DecisionSubstantially Equivalent, Jan 10, 2002
ReceivedDec 3, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013969

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.