ClearanceBrief
510(k) K884857 ยท FDF Colonoscope And Accessories, Flexible/Rigid

COLONOSCOPE GUIDING TUBE DEVICE

ApplicantMill-Rose Laboratory, Mentor OH, US
DecisionSubstantially Equivalent, Mar 17, 1989
ReceivedNov 21, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884857

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.