ClearanceBrief
510(k) K111808 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological

SONOLITH I-MOVE

ApplicantEdap Tms France, Washington, D.C. DC, US
DecisionSubstantially Equivalent, Aug 1, 2011
ReceivedJun 27, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111808

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.