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Medical Devices; Immunology and Microbiology Devices; Classification of Ribonucleic Acid Preanalytical Systems

fda-device · Food and Drug Administration · Rule · Published 2005-08-25 · Effective 2005-09-26 · 70 FR 49862

Document

Document number
05-16914
Federal Register citation
70 FR 49862
CFR reference
21 CFR 866
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2005-08-25
Effective date
2005-09-26
HHS docket
Docket No. 2005N-0263

Abstract

The Food and Drug Administration (FDA) is classifying ribonucleic acid (RNA) preanalytical systems into class II (special controls). The special control that will apply to the device is the guidance document entitled "Class II Special Controls Guidance Document: RNA Preanalytical Systems (RNA Collection, Stabilization, and Purification Systems for RT-PCR Used in Molecular Diagnostic Testing)." The agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device. Elsewhere in this issue of the Federal Register, FDA is announcing the availability of a guidance document that will serve as the special control for the device.

Source

Authoritative
Federal Register document
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