ClearanceBrief
510(k) K032958 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological

PIEZOLITH 3000 LITHOTRIPTER, MODEL 3000

ApplicantUnited Medical Systems, Inc., Washington DC, US
DecisionSubstantially Equivalent, Feb 17, 2004
ReceivedSep 22, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032958

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.