federal_register: 2013-11628
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2013-11628 | Medical Devices; General Hospital and Personal Use Monitoring Devices; Classification of the Ingestible Event Marker | Rule | The Food and Drug Administration (FDA) is classifying the ingestible event marker into class II (special controls). The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device. | 2013-05-16 | 2013 | 5 | https://www.federalregister.gov/documents/2013/05/16/2013-11628/medical-devices-general-hospital-and-personal-use-monitoring-devices-classification-of-the | https://www.govinfo.gov/content/pkg/FR-2013-05-16/pdf/2013-11628.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is classifying the ingestible event marker into class II (special controls). The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and... |