ClearanceBrief
510(k) K071113 ยท GZI Stimulator, Neuromuscular, External Functional

RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053

ApplicantRestorative Therapies, Inc., Baltimore MD, US
DecisionSubstantially Equivalent, Jul 5, 2007
ReceivedApr 20, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071113

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.