ClearanceBrief
510(k) K974796 ยท FFK Lithotriptor, Electro-Hydraulic

LITHOSPEC(TM) INTRACORPOREAL LITHOTRIPTER

ApplicantMedispec, Ltd., Montgomery Village MD, US
DecisionSubstantially Equivalent, Mar 12, 1998
ReceivedDec 22, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974796

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.