{"url_path":"/fda/devices/510k/K252702","section_key":"summary","section_title":"510(k) Clearance: Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-11…","topic":"fda","document":{"doc_type":"510k-clearance","doc_date":"2026-05-28","source_url":"https://api.fda.gov/device/510k.json?search=k_number:%22K252702%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Bioptimal International Pte. , Ltd."},"word_count":66,"has_tables":false,"body_markdown":null}