federal_register: 04-28251
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 04-28251 | Medical Devices; Obstetrical and Gynecological Devices; Classification of the Assisted Reproduction Laser System | Rule | The Food and Drug Administration (FDA) is classifying the assisted reproduction laser system into class II (special controls). The special control that will apply to the device is the guidance document entitled "Class II Special Controls Guidance Document: Assisted Reproduction Laser Systems." The agency is classifying this device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device. Elsewhere in this issue of the Federal Register, FDA is publishing a notice of availability of the guidance document that is the special control for this device. | 2004-12-28 | 2004 | 12 | https://www.federalregister.gov/documents/2004/12/28/04-28251/medical-devices-obstetrical-and-gynecological-devices-classification-of-the-assisted-reproduction | https://www.govinfo.gov/content/pkg/FR-2004-12-28/pdf/04-28251.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is classifying the assisted reproduction laser system into class II (special controls). The special control that will apply to the device is the guidance document entitled "Class II Special Controls Guidance... |