← Back to FR Documents
Final Rule

Medical Devices; Immunology and Microbiology Devices; Classification of the Inherited Nucleotide Repeat Disorder Deoxyribonucleic Acid Test

Final amendment; final order.

📖 Research Context From Federal Register API

Summary:

The Food and Drug Administration (FDA, Agency, or we) is classifying the inherited nucleotide repeat disorder DNA test 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 inherited nucleotide repeat disorder DNA test's 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.

Key Dates
Citation: 90 FR 22629
This order is effective May 29, 2025. The classification was applicable on February 21, 2020.
Public Participation
Topics:
Biologics Laboratories Medical devices

Document Details

Document Number2025-09641
FR Citation90 FR 22629
TypeFinal Rule
PublishedMay 29, 2025
Effective DateMay 29, 2025
RIN-
Docket IDDocket No. FDA-2025-N-1183
Pages22629–22632 (4 pages)
Text FetchedNo

Agencies & CFR References

CFR References:

Linked CFR Parts

PartNameAgency
21 CFR 866 Immunology and Microbiology Devices... -

Paired Documents

TypeProposedFinalMethodConf
No paired documents

External Links

Full Text

Text Not Yet Fetched

The full text for this document hasn't been fetched yet. The system will automatically retrieve it during the next processing cycle.