ClearanceBrief
510(k) K162622 ยท FDF Colonoscope And Accessories, Flexible/Rigid

Fujifilm Endoscope Models EC-600HL and EC-600LS

ApplicantFujifilm Medical Systems U.S.A, Inc., Wayne NJ, US
DecisionSubstantially Equivalent, Oct 18, 2016
ReceivedSep 20, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K162622

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.