ClearanceBrief
510(k) K051637 ยท FCK Instrument, Biopsy, Suction

DSNARE, MODEL 00711087

ApplicantUnited States Endoscopy Group, Inc., Mentor OH, US
DecisionSubstantially Equivalent, Oct 31, 2005
ReceivedJun 20, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051637

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.