510(k) Report

FDA applicant

Line Imaging Systems

Atlanta, GA1 decision1994–19940 recalls

FDA records 1 decision for Line Imaging Systems (Atlanta, GA) in 1994: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). 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 Line Imaging Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Line Imaging Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Line Imaging Systems 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?

  • LLZSystem, Image Processing, Radiological1decision

Who builds on its devices?

Later devices cite its devices 4 times; 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.

  • K936179Winrad Teleradiology SystemLine Imaging Systems · 19944cite it

What has FDA decided for it lately?

  • K936179Winrad Teleradiology SystemLine Imaging Systems · 1994

The one decision as Line Imaging Systems →

Other applicant names beginning “Line”

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

Line One Laboratories 6Line One Laboratories & Trading Co. 3Line Ind.(Shanghai) Co., Ltd. 1