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Medical Devices; Anesthesiology Devices; Classification of the Ventilatory Electrical Impedance Tomograph

fda-device · Food and Drug Administration · Rule · Published 2019-04-15 · Effective 2019-04-15 · 84 FR 15096

Document

Document number
2019-07463
Federal Register citation
84 FR 15096
CFR reference
21 CFR 868
Type
Rule
Action
Final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2019-04-15
Effective date
2019-04-15
HHS docket
Docket No. FDA-2019-N-0647

Abstract

The Food and Drug Administration (FDA or we) is classifying the ventilatory electrical impedance tomograph into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the ventilatory electrical impedance tomograph's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.

Source

Authoritative
Federal Register document
Machine
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