section_subject: "Percutaneous nerve stimulator for substance use disorders."
cfr_reference: "21 CFR 882.5896"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 800 to 1299"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
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(a)Identification. A percutaneous nerve stimulator for substance use disorders is a device that stimulates nerves percutaneously to aid in the reduction of withdrawal symptoms associated with substance use disorders.
(b)Classification. Class II (special controls). The special controls for this device are:
(1)The patient-contacting components of the device must be demonstrated to be biocompatible.
(2)Electromagnetic compatibility and electrical, mechanical, and thermal safety testing must be performed.
(3)Electrical performance testing of the device and electrodes must be conducted to validate the specified electrical output and duration of stimulation of the device.
(4)Software verification, validation, and hazard analysis must be performed.
(5)Sterility testing of the percutaneous components of the device must be performed.
(6)Shelf life testing must be performed to demonstrate continued sterility, package integrity, and device functionality over the specified shelf life.