ClearanceBrief
510(k) K090750 ยท GZI Stimulator, Neuromuscular, External Functional

RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581

ApplicantRestorative Therapies, Inc., Baltimore MD, US
DecisionSubstantially Equivalent, Aug 5, 2009
ReceivedMar 20, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090750

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.