Changeflow GovPing Healthcare & Life Sciences Variance Application from BF Light Shows, Michigan
Routine Notice Added Final

Variance Application from BF Light Shows, Michigan

Favicon for www.regulations.gov Regs.gov: Food and Drug Administration
Published
Detected
Email

Summary

FDA CDRH received a variance application from BF Light Shows, a Michigan-based entity, seeking regulatory relief or alternative compliance pathway under FDA electronic product radiation control requirements. The application was filed under docket FDA-2026-V-2878.

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

What changed

FDA's Center for Devices and Radiological Health (CDRH) received a variance application from BF Light Shows located in Michigan. The variance application relates to FDA requirements governing electronic products that emit radiation, likely seeking authorization to use alternative compliance methods or obtain an exemption from standard radiation safety standards for light show equipment.

BF Light Shows should await FDA review and determination on their variance request. Interested parties may access the full application materials through the Regulations.gov docket FDA-2026-V-2878. The variance, if approved, would allow deviation from standard requirements applicable to the specific light show electronic products at issue.

Archived snapshot

Apr 3, 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 1

Variance Application from BF Light Shows

More Information
- Author(s) CDRH
Download

Get daily alerts for Regs.gov: Food and Drug Administration

Daily digest delivered to your inbox.

Free. Unsubscribe anytime.

About this page

What is GovPing?

Every important government, regulator, and court update from around the world. One place. Real-time. Free. Our mission

What's from the agency?

Source document text, dates, docket IDs, and authority are extracted directly from FDA.

What's AI-generated?

The summary, classification, recommended actions, deadlines, and penalty information are AI-generated from the original text and may contain errors. Always verify against the source document.

Last updated

Classification

Agency
FDA
Published
January 7th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
Docket No. FDA-2026-V-2878
Docket
FDA-2026-V-2878

Who this affects

Applies to
Medical device makers
Industry sector
3341 Computer & Electronics Manufacturing
Activity scope
Electronic Product Radiation Control
Geographic scope
United States US

Taxonomy

Primary area
Medical Devices
Operational domain
Compliance
Compliance frameworks
FDA 21 CFR Part 11
Topics
Electronic Products Radiation Safety

Get alerts for this source

We'll email you when Regs.gov: Food and Drug Administration publishes new changes.

Free. Unsubscribe anytime.

You're subscribed!