Medical Device Classification Procedures; Reclassification Petition: Content and Form; Technical Amendment
Information
Type
Rule
Regulated products
Medical Devices
Published
December 24, 2014
Last updated
December 24, 2014
Description
Document number 2014-30141. The Food and Drug Administration (FDA) is amending its regulations for petitioning for device reclassification to update mailing addresses for the petitions. This action is being taken to improve the accuracy of the regulations.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)