Changeflow GovPing Government & Legislation Variance Application from Anthony Ritzko
Routine Notice Added Final

Variance Application from Anthony Ritzko

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Published March 24th, 2026
Detected March 25th, 2026
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Summary

The GSA has posted a variance application from Anthony Ritzko, filed on March 24, 2026. The application is related to medical device regulations and has been submitted by CDRH.

What changed

This document is a notice regarding a variance application submitted by Anthony Ritzko to the CDRH (Center for Devices and Radiological Health), which falls under the GSA's purview on Regulations.gov. The application itself is restricted due to Personally Identifiable Information, but a redacted version is available for download. This filing represents a specific request for a deviation from standard regulations concerning medical devices.

Compliance officers should note that this is an individual variance request and does not represent a change in overarching regulations. While the application is filed, the content is restricted, and the primary action for compliance teams is to be aware of its existence and its filing date. No immediate compliance actions or deadlines are imposed by this notice.

Source document (simplified)

Content

There are no documents available to view or download

Attachments 2

Variance Application from Anthony Ritzko

Restricted: Personally Identifiable Information

More Information
- Author(s) CDRH

Variance Application from Anthony Ritzko_Redacted

More Information
- Author(s) CDRH
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Classification

Agency
GSA
Published
March 24th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2025-V-4992-0001
Docket
FDA-2025-V-4992

Who this affects

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

Taxonomy

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

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