DevicePMAs@therightstef:P910073_S043 JSONTXT

{"project":"PMA_MER","denotations":[{"id":"T1","span":{"begin":0,"end":8},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25425"},{"id":"T2","span":{"begin":49,"end":54},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35016"},{"id":"T3","span":{"begin":121,"end":125},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C42614"},{"id":"T4","span":{"begin":148,"end":152},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25552"},{"id":"T5","span":{"begin":230,"end":243},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70911"},{"id":"T6","span":{"begin":278,"end":287},"obj":"http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70669"}],"text":"Approval for addition of an eptfe coating to the shock coils. The device, as modified, will be marketed under the trade name endotak reliance g/sg lead models and is indicated for providing pacing and rate-sensing and to deliver cardioversion and defibrillation shocks for icd automatic implantable cardioverter defibrillator systems."}