{"url_path":"/fda/devices/510k/K254200","section_key":"summary","section_title":"510(k) Clearance: Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI…","topic":"fda","document":{"doc_type":"510k-clearance","doc_date":"2026-05-05","source_url":"https://api.fda.gov/device/510k.json?search=k_number:%22K254200%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Wenzhou Lingfeng Electronic Technology Co., Ltd."},"word_count":85,"has_tables":false,"body_markdown":null}