← HHS Federal Register rules

Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Blood Collection Device for Cell-Free Nucleic Acids

fda-device · Food and Drug Administration · Rule · Published 2024-09-09 · Effective 2024-09-09 · 89 FR 72982

Document

Document number
2024-20254
Federal Register citation
89 FR 72982
CFR reference
21 CFR 862
Type
Rule
Action
Final amendment; final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2024-09-09
Effective date
2024-09-09
HHS docket
Docket No. FDA-2024-N-4086

Abstract

The Food and Drug Administration (FDA, Agency, or we) is classifying the blood collection device for cell-free nucleic acids into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the blood collection device for cell-free nucleic acids' classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.

Source

Authoritative
Federal Register document
Machine
JSON-LD · Markdown