Changeflow GovPing Healthcare & Life Sciences FDA Acknowledgment Letter to Mykyta Sukhenko
Routine Notice Added Final

FDA Acknowledgment Letter to Mykyta Sukhenko

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Summary

The Food and Drug Administration (FDA) has posted an acknowledgment letter sent to Mykyta Sukhenko regarding a submission. The letter, authored by the Center for Devices and Radiological Health (CDRH), indicates a formal receipt of information or documentation.

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What changed

This document consists of an acknowledgment letter from the FDA's Division of Management and Budget (DMB) to Mykyta Sukhenko, dated March 20, 2026. The letter, originating from the Center for Devices and Radiological Health (CDRH), confirms receipt of a submission. While the content is restricted due to Personally Identifiable Information (PII) in one version, a redacted version is also available.

This notice serves as confirmation of FDA's receipt of a submission from Mykyta Sukhenko. Regulated entities, particularly those interacting with the CDRH, should note this as a standard procedural communication. No immediate action is required by other parties based on this acknowledgment, but it signifies that a submission has entered the FDA's review process.

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

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Attachments 2

Acknowledgment Letter from FDA DMB to Mykyta Sukhenko

Restricted: Personally Identifiable Information

More Information
- Author(s) CDRH

Acknowledgment Letter from FDA DMB to Mykyta Sukhenko_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-2026-V-1610-0002
Docket
FDA-2026-V-1610-0002

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
Compliance
Compliance frameworks
FDA 21 CFR Part 11
Topics
Medical Devices

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