Medical Device Classification Procedures; Reclassification Petition: Content and Form; Technical Amendment
fda-device · Food and Drug Administration · Rule · Published 2014-12-24 · Effective 2014-12-24 · 79 FR 77387
Document
Document number
2014-30141
Federal Register citation
79 FR 77387
CFR reference
21 CFR 860
Type
Rule
Action
Final rule; technical amendments.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2014-12-24
Effective date
2014-12-24
HHS docket
Docket No. FDA-2013-N-1529
Abstract
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.