ClearanceBrief
510(k) K041233 ยท HRX Arthroscope

ARTHROJET XT

ApplicantHydrocision, Inc., Hopkonton MA, US
DecisionSubstantially Equivalent, Jul 28, 2004
ReceivedMay 10, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K041233

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.