Changeflow GovPing Healthcare & Life Sciences FDA Variance Application from Kyle Cummings
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FDA Variance Application from Kyle Cummings

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Summary

The FDA has posted a variance application submitted by Kyle Cummings. The application is from the CDRH (Center for Devices and Radiological Health) and is available for review, with a redacted version provided for download. No specific details of the variance are available in the provided text.

Published by FDA on regulations.gov . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

The Food and Drug Administration (FDA) has published a variance application submitted by Kyle Cummings, identified by docket number FDA-2025-V-2665-0001. The application, authored by the Center for Devices and Radiological Health (CDRH), is available for public viewing, with a redacted version provided for download. The document itself contains no substantive information beyond the metadata of the application.

As this is a notice of a filed application with no accompanying rule or guidance, there are no immediate compliance actions required for regulated entities. The availability of the redacted application suggests a potential for future transparency regarding specific variances granted or considered by the FDA. Compliance officers should note the docket number for tracking purposes if related actions or rules emerge.

Archived snapshot

Mar 21, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Content

There are no documents available to view or download

Attachments 2

Variance Application from Kyle Cummings

Restricted: Personally Identifiable Information

More Information
- Author(s) CDRH

Variance Application from Kyle Cummings - Redacted

More Information
- Author(s) CDRH
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Last updated

Classification

Agency
FDA
Published
March 20th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2025-V-2665-0001
Docket
FDA-2025-V-2665-0001

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Medical Device Approval
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Compliance frameworks
FDA 21 CFR Part 11
Topics
Medical Devices

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