510(k) Report

FDA applicant

James D Rusin MD, MBA

Anoka, MN1 decision2002–20020 recalls

FDA records 1 decision for James D Rusin MD, MBA (Anoka, MN) in 2002: 1 510(k) clearance. All are in product code NHM (Sheet, Recording, Breast Examination). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, obstetrics and gynecology panel, where it files most

How often FDA has decided James D Rusin MD, MBA’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for James D Rusin MD, MBA since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — James D Rusin MD, MBA by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NHMSheet, Recording, Breast Examination1decision

What has FDA decided for it lately?

  • K014300SafetouchJames D Rusin MD, MBA · 2002

The one decision as James D Rusin MD, MBA →

Other applicant names beginning “James”

FDA records each applicant name separately; these may or may not be the same firm.

James River Corp. 15James L. Geraci & Associates, Inc. 5James Leckey Design 2James K. Brannon 2James J. Schramm 1James R. Powell 1James Nguyen 1James P Boyd 1James Consolidated, Inc. 1James J. Lally 1James Alexander Corp. 1James Korea Co., Ltd. 1