Medical Devices; Immunology and Microbiology Devices; Classification of Plasmodium Species Antigen Detection Assays
fda-device · Food and Drug Administration · Rule · Published 2008-05-20 · Effective 2008-06-19 · 73 FR 29052
Document
Document number
E8-11263
Federal Register citation
73 FR 29052
CFR reference
21 CFR 866
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2008-05-20
Effective date
2008-06-19
HHS docket
Docket No. FDA-2008-N-0231
Abstract
The Food and Drug Administration (FDA) is classifying Plasmodium species antigen detection assays 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: Plasmodium Species Antigen Detection Assays." 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 the guidance document that will serve as the special control for this device.