510(k) Report

FDA applicant

Sonovision Corp.

Hasbrouck Heights, NJ1 decision2000–20000 recalls

FDA records 1 decision for Sonovision Corp. (Hasbrouck Heights, NJ) in 2000: 1 510(k) clearance. All are in product code OXO (Image-Intensified Fluoroscopic X-Ray System…). 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 Sonovision Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sonovision Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sonovision Corp. 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?

  • OXOImage-Intensified Fluoroscopic X-Ray System, Mobile1decision

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.

  • K993092Sonada Ultrasound SystemSonovision Corp. · 20001cites it

What has FDA decided for it lately?

  • K993092Sonada Ultrasound SystemSonovision Corp. · 2000

The one decision as Sonovision Corp. →