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General Hospital and Personal Use Devices: Renaming of Pediatric Hospital Bed Classification and Designation of Special Controls for Pediatric Medical Crib; Classification of Medical Bassinet

fda-device · Food and Drug Administration · Rule · Published 2016-12-19 · Effective 2017-01-18 · 81 FR 91731

Document

Document number
2016-30193
Federal Register citation
81 FR 91731
CFR reference
21 CFR 880
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2016-12-19
Effective date
2017-01-18
HHS docket
Docket No. FDA-2015-N-0701

Abstract

The Food and Drug Administration (FDA) is issuing a final rule to rename pediatric hospital beds as pediatric medical cribs and establish special controls for these devices. FDA is also establishing a separate classification regulation for medical bassinets, previously under the pediatric hospital bed classification regulation, as a class II (special controls) device. In addition, this rule continues to allow both devices to be exempt from premarket notification and use of the device in traditional health care settings and permits prescription use of pediatric medical cribs and bassinets outside of traditional health care settings.

Source

Authoritative
Federal Register document
Machine
JSON-LD · Markdown