# Medical Devices; Technical Amendment
> **Food and Drug Administration** · Final rule; technical amendment. · Published 2020-04-02 · Effective 2020-04-01 · 85 FR 18444
## Document
- **Document number:** 2020-06278
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 85 FR 18444
- **CFR reference:** 21 CFR 862
- **Publication date:** 2020-04-02
- **Effective date:** 2020-04-01
- **HHS docket:** Docket No. FDA-2020-N-0011
## Abstract

The Food and Drug Administration (FDA or Agency) is amending certain medical device regulations to accurately reflect the devices exempted from premarket notification (510(k)) as indicated in the lists published on April 13, 2017, and July 11, 2017. FDA published a final amendment, final order in the Federal Register of December 30, 2019 ("Final Order") codifying the two Federal Register notices. The present revisions are necessary to correct editorial errors to ensure that the codified is consistent with the exemptions in the Federal Register notices. The rule does not impose any new regulatory requirements on affected parties. This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2020/04/02/2020-06278/medical-devices-technical-amendment)
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