ClearanceBrief
510(k) K133752 ยท ELC Scaler, Ultrasonic

SONENDO OMNICLEAN ENDOTHERPAY SYSTEM CONSOLE, SONENDO OMNICLEAN MOLAR PROCEDURE KIT

ApplicantSonendo, Inc., Laguna Hills CA, US
DecisionSubstantially Equivalent, May 15, 2014
ReceivedDec 9, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133752

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.