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Medical Devices; Obstetrical and Gynecological Devices; Classification of Computerized Labor Monitoring System

fda-device · Food and Drug Administration · Rule · Published 2007-04-24 · Effective 2007-05-24 · 72 FR 20225

Document

Document number
E7-7702
Federal Register citation
72 FR 20225
CFR reference
21 CFR 884
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2007-04-24
Effective date
2007-05-24
HHS docket
Docket No. 2007N-0120

Abstract

The Food and Drug Administration (FDA) is classifying the computerized labor monitoring systems into class II (special controls). Elsewhere in this issue of the Federal Register, FDA is announcing the availability of a guidance document entitled, "Guidance for Industry and FDA Staff; Class II Special Controls Guidance Document: Computerized Labor Monitoring Systems," which will serve as the special controls for these devices. The agency is classifying these devices into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of these devices.

Source

Authoritative
Federal Register document
Machine
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