⚖️FDA Proposes Information Collection on Medical Device Accessories
Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device Accessories
Summary
The Food and Drug Administration (FDA, Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection associated with medical device accessory classification requests.
Agencies
- Health and Human Services Department
- Food and Drug Administration
Business Impact
$$ - Med
The text discusses the FDA's proposed information collection regarding medical device accessories, which requires compliance from manufacturers and may impose additional regulatory burdens. It invites comments that could influence future classification processes and regulatory requirements, directly impacting business operations within the medical device industry.