{"url_path":"/fda/devices/510k/K261412","section_key":"summary","section_title":"510(k) Clearance: V8/XV8/XH8/H8/cV8/V8 ONE/XV8 ONE/XH8 ONE/H8 ONE/cV8 ONE Diagnostic Ultrasound System; V7/XV7/XH7/H7/cV7/V7 ONE/XV7 ONE/H7 ONE/XH7 ONE/cV7 ONE Diagnostic Ultrasound System; V6/XV6/XH6/H6/cV6/V6 ONE/XV6 ONE/H6 ONE/XH6 ONE/cV6 ONE Diagnostic Ultrasound System; V5/XV5/XH5/H5/cV5 Diagnostic Ultrasound System; V4/XV4/XH4/H4/cV4 Diagnostic Ultrasound System; — Samsung Medison Co., Ltd.","topic":"fda","document":{"doc_type":"510k-clearance","doc_date":"2026-07-28","source_url":"https://api.fda.gov/device/510k.json?search=k_number:%22K261412%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Samsung Medison Co., Ltd."},"word_count":63,"has_tables":false,"body_markdown":null}