{"url_path":"/fda/devices/510k/K260846","section_key":"summary","section_title":"510(k) Clearance: Diagnostic Ultrasound System (MU9);Diagnostic Ultrasound System (MU9S);Diagnostic Ultrasound System (MU9T);Diagnostic Ultrasound System (MU9 Exp);Diagnostic Ultrasound System (MU9 Pro);Diagnostic Ultrasound System (MU9 Super);Diagnostic Ultrasound System (MU9P);Diagnostic Ultrasound System (MU9A);Diagnostic Ultrasound System (MU7);Diagnostic Ultrasound System (MU7S);Diagnostic U…","topic":"fda","document":{"doc_type":"510k-clearance","doc_date":"2026-05-11","source_url":"https://api.fda.gov/device/510k.json?search=k_number:%22K260846%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Shenzhen Mindray Bio-Medical Electronics Co., Ltd."},"word_count":75,"has_tables":false,"body_markdown":null}