510(k) Report

FDA applicant

Northern Virginia Radiology and Nuclear Medicine

Falls Church, VA1 decision1991–19910 recalls

FDA records 1 decision for Northern Virginia Radiology and Nuclear Medicine (Falls Church, VA) in 1991: 1 510(k) clearance. All are in product code HRX (Arthroscope). 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, orthopedic panel, where it files most

How often FDA has decided Northern Virginia Radiology and Nuclear Medicine’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northern Virginia Radiology and Nuclear Medicine since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Northern Virginia Radiology and Nuclear Medicine 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?

  • HRXArthroscope1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K911974PGK Stereotactic DeviceNorthern Virginia Radiology and Nuclear Medicine · 19911cites it

What has FDA decided for it lately?

  • K911974PGK Stereotactic DeviceNorthern Virginia Radiology and Nuclear Medicine · 1991

The one decision as Northern Virginia Radiology and Nuclear Medicine →