ClearanceBrief
510(k) K100610 ยท ONG Powered Laser Surgical Instrument With MicrobeamFractional Output

LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS

ApplicantLutronic Corporation, North Reading MA, US
DecisionSubstantially Equivalent, Jan 20, 2011
ReceivedMar 3, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100610

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.