# Radiological Health Regulations; Amendments to Records and Reports for Radiation Emitting Electronic Products; Amendments to Performance Standards for Diagnostic X-ray, Laser, and Ultrasonic Products
> **Food and Drug Administration** · Final rule. · Published 2023-01-20 · Effective 2023-02-21 · 88 FR 3638
## Document
- **Document number:** 2023-00922
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 88 FR 3638
- **CFR reference:** 21 CFR 1000
- **Publication date:** 2023-01-20
- **Effective date:** 2023-02-21
- **HHS docket:** Docket No. FDA-2018-N-3303
## Abstract

The Food and Drug Administration (FDA, Agency, or we) is amending and repealing parts of the radiological health regulations covering recommendations for radiation protection during medical procedures, certain records and reporting for electronic products, and performance standards for diagnostic x-ray systems and their major components, laser products, and ultrasonic therapy products. The Agency is taking this action to clarify and update the regulations to reduce regulatory requirements that are outdated and duplicate other means to better protect the public health against harmful exposure to radiation emitting electronic products and medical devices.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2023/01/20/2023-00922/radiological-health-regulations-amendments-to-records-and-reports-for-radiation-emitting-electronic)
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