ClearanceBrief
510(k) K961536 ยท GDB Endoscope, Fiber Optic

FLEXSCOPE

ApplicantMatrix Medica, Inc., Burnsville MN, US
DecisionSubstantially Equivalent, Sep 18, 1996
ReceivedApr 22, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961536

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.