federal_register: 2017-21982
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2017-21982 | Medical Devices; Neurological Devices; Classification of Cranial Motion Measurement Device; Correction | Rule | The Food and Drug Administration (FDA) is correcting a final order entitled "Medical Devices; Neurological Devices; Classification of Cranial Motion Measurement Device" that appeared in the Federal Register of July 28, 2017. The final order was published with an incorrect statement in the preamble about whether FDA planned to exempt the device from premarket notification requirements. This document corrects that error. | 2017-10-12 | 2017 | 10 | https://www.federalregister.gov/documents/2017/10/12/2017-21982/medical-devices-neurological-devices-classification-of-cranial-motion-measurement-device-correction | https://www.govinfo.gov/content/pkg/FR-2017-10-12/pdf/2017-21982.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is correcting a final order entitled "Medical Devices; Neurological Devices; Classification of Cranial Motion Measurement Device" that appeared in the Federal Register of July 28, 2017. The final order was... |