ClearanceBrief
510(k) K992477 ยท FDI Snare, Flexible

ROTOSNARE

ApplicantInscope, LLC, Miami FL, US
DecisionSubstantially Equivalent, Aug 24, 1999
ReceivedJul 26, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992477

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.