510(k) Report

FDA applicant

Quicksilver Systems, Inc.

Rockville, MD1 decision1995–19950 recalls

FDA records 1 decision for Quicksilver Systems, Inc. (Rockville, MD) in 1995: 1 510(k) clearance. All are in product code LMD (System, Digital Image Communications…). 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, radiology panel, where it files most

How often FDA has decided Quicksilver Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Quicksilver Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Quicksilver Systems, Inc. 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?

  • LMDSystem, Digital Image Communications, Radiological1decision

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.

  • K953163Quick Read 2000 (QR2000)Quicksilver Systems, Inc. · 19951cites it

What has FDA decided for it lately?

  • K953163Quick Read 2000 (QR2000)Quicksilver Systems, Inc. · 1995

The one decision as Quicksilver Systems, Inc. →