ClearanceBrief
510(k) K932997 ยท KOJ Airbrush

MICROPREP CAVITY PREPERATION SYSTEM

ApplicantSunrise Technologies, Inc., Fremont CA, US
DecisionSubstantially Equivalent, Apr 25, 1994
ReceivedJun 18, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932997

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.