{"abstract":"The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of July 28, 2010 (75 FR 44267). The document reopened the comment period for a notice of availability of draft guidance documents for 11 neurological and physical medicine devices. The document was published with an inadvertent error. This document corrects that error.","action":"Notice; correction.","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2010/08/06/2010-19355.html","cfr_references":[],"citation":"75 FR 47604","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":null,"disposition_notes":null,"docket_ids":["Docket No. FDA-2009-D-0495"],"dockets":[],"document_number":"2010-19355","effective_on":null,"end_page":47604,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2010/08/06/2010-19355.xml","html_url":"https://www.federalregister.gov/documents/2010/08/06/2010-19355/draft-guidance-for-industry-and-food-and-drug-administration-staff-medical-devices-neurological-and","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2010-19355?publication_date=2010-08-06","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2010-08-06/2010-19355/mods.xml","not_received_for_publication":null,"page_length":1,"page_views":{"count":19,"last_updated":"2026-04-04 16:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2010-08-06/pdf/2010-19355.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2010-08-06","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2010/08/06/2010-19355.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"checked_regulationsdotgov_at":"2010-08-26T11:22:08Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":47604,"subtype":null,"title":"Draft Guidance for Industry and Food and Drug Administration Staff; Medical Devices; Neurological and Physical Medicine Device Guidance Document; Reopening of Comment Period; Correction","toc_doc":"Medical Devices; Neurological and Physical Medicine Device Guidance; Correction","toc_subject":"Draft Guidance for Industry and Food and Drug Administration Staff:","topics":[],"type":"Notice","volume":75}