← HHS Federal Register rules

Medical Devices; Ear, Nose, and Throat Devices; Classification of the Transcutaneous Air Conduction Hearing Aid System

fda-device · Food and Drug Administration · Rule · Published 2002-11-07 · Effective 2002-11-07 · 67 FR 67789

Document

Document number
02-28398
Federal Register citation
67 FR 67789
CFR reference
21 CFR 874
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2002-11-07
Effective date
2002-11-07
HHS docket
Docket No. 02P-0241

Abstract

The Food and Drug Administration (FDA) is classifying the transcutaneous air conduction hearing aid system (TACHAS) into class II (special controls). 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. The agency is taking this action in response to a petition submitted under the Federal Food, Drug, and Cosmetic Act (the act) as amended by the Medical Device Amendments of 1976 (the amendments), the Safe Medical Devices Act of 1990, and the Food and Drug Administration Modernization Act of 1997 (FDAMA). The agency is classifying this device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.

Source

Authoritative
Federal Register document
Machine
JSON-LD · Markdown