Changeflow GovPing Healthcare & Life Sciences FDA Variance Application from Mykyta Sukhenko
Routine Notice Added Final

FDA Variance Application from Mykyta Sukhenko

Email

Summary

The FDA has posted a variance application submitted by Mykyta Sukhenko. The application is restricted due to personally identifiable information, but a redacted version is available for review. This notice serves to inform the public of the application's existence.

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

What changed

The FDA has made publicly available a variance application submitted by Mykyta Sukhenko, identified by docket number FDA-2026-V-1610-0001. While the full application contains restricted personally identifiable information, a redacted version has also been provided. The application was authored by CDRH (Center for Devices and Radiological Health).

This filing is primarily informational. Regulated entities should note the existence of this variance application and may review the redacted version if interested in the specific details or the nature of the variance sought. No immediate action is required from compliance officers based on this notice, as it pertains to a specific applicant's request.

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 Mykyta Sukhenko

Restricted: Personally Identifiable Information

More Information
- Author(s) CDRH

Variance Application from Mykyta Sukhenko_Redacted

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
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2026-V-1610-0001
Docket
FDA-2026-V-1610-0001

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Regulatory Submissions
Geographic scope
United States US

Taxonomy

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

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!