ClearanceBrief
510(k) K020688 ยท HRX Arthroscope

HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR

ApplicantHydrocision, Inc., Hopkonton MA, US
DecisionSubstantially Equivalent, Apr 3, 2002
ReceivedMar 4, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020688

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.