ClearanceBrief
510(k) K163247 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider

ApplicantLaurimed, LLC, Redwood City CA, US
DecisionSubstantially Equivalent, Mar 9, 2017
ReceivedNov 18, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K163247

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.