# Medical Devices; Anesthesiology Devices; Classification of Devices to Relieve Upper Airway Obstruction; Correction
> **Food and Drug Administration** · Final rule; correction. · Published 2000-08-03 · Effective 2000-08-03 · 65 FR 47669
## Document
- **Document number:** 00-19593
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 65 FR 47669
- **CFR reference:** 21 CFR 868
- **Publication date:** 2000-08-03
- **Effective date:** 2000-08-03
- **HHS docket:** Docket No. 00P-1117
## Abstract

The Food and Drug Administration (FDA) is correcting a final rule that appeared in the Federal Register of June 23, 2000 (65 FR 39098). The document classified devices to relieve acute upper airway obstruction. These type devices were classified into class II. The preamble to the final rule correctly states that the devices were exempt from premarket notification, but this exemption was not reflected in the regulatory text. This document corrects that error.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2000/08/03/00-19593/medical-devices-anesthesiology-devices-classification-of-devices-to-relieve-upper-airway-obstruction)
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