510(k) Report

FDA applicant

E For M Imaging Systems Div., Marquette Electronic

Torrance, CA2 decisions1996–19980 recalls

FDA records 2 decisions for E For M Imaging Systems Div., Marquette Electronic (Torrance, CA) from 1996 to 1998: 2 510(k) clearances. Most are in product codes LMB (Device, Digital Image Storage, Radiological) and LLZ (System, Image Processing, Radiological). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 E For M Imaging Systems Div., Marquette Electronic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E For M Imaging Systems Div., Marquette Electronic since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — E For M Imaging Systems Div., Marquette Electronic 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?

  • LMBDevice, Digital Image Storage, Radiological1decision
  • LLZSystem, Image Processing, Radiological1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

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.

  • K955184AcculupeE For M Imaging Systems Div., Marquette Electronic · 19961cites it

What has FDA decided for it lately?

  • K974504EPSE For M Imaging Systems Div., Marquette Electronic · 1998
  • K955184AcculupeE For M Imaging Systems Div., Marquette Electronic · 1996

All 2 as E For M Imaging Systems Div., Marquette Electronic →