ClearanceBrief
510(k) K092202 ยท IPF Stimulator, Muscle, Powered

ESWALLOW DYSPHAGIA THERAPY KIT, PMI DYSPHAGIA THERAPY KIT

ApplicantEswallow USA, Naples FL, US
DecisionSubstantially Equivalent, Feb 10, 2011
ReceivedJul 22, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092202

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.