# Medical Devices; Radiology Devices; Reclassification of Bone Sonometers
> **Food and Drug Administration** · Final rule; correction. · Published 2008-08-14 · 73 FR 47523
## Document
- **Document number:** E8-18792
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 73 FR 47523
- **CFR reference:** 21 CFR 892
- **Publication date:** 2008-08-14
- **HHS docket:** Docket No. FDA-2005-N-0346
## Abstract

The Food and Drug Administration (FDA) is correcting a final rule that appeared in the Federal Register of July 17, 2008 (73 FR 40967). The final rule reclassified bone sonometer devices from class III into class II, subject to special controls. The document contained an inadvertent error regarding the impact of the final rule on small businesses. This document corrects that error.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2008/08/14/E8-18792/medical-devices-radiology-devices-reclassification-of-bone-sonometers)
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