510(k) Report

FDA applicant

S & S Inficon, Inc.

Liverpool, NY4 decisions1990–19920 recalls

FDA records 4 decisions for S & S Inficon, Inc. (Liverpool, NY) from 1990 to 1992: 4 510(k) clearances. Most are in product codes IYE (Accelerator, Linear, Medical) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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 S & S Inficon, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for S & S Inficon, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — S & S Inficon, 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?

  • IYEAccelerator, Linear, Medical2decisions
  • JAASystem, X-Ray, Fluoroscopic, Image-Intensified2decisions

Who builds on its devices?

Later devices cite its devices 2 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.

  • K911454FC2000S & S Inficon, Inc. · 19912cite it

What has FDA decided for it lately?

  • K922977ExposetS & S Inficon, Inc. · 1992
  • K920455Theraview Digital Portal Imaging Computer (Mod.)S & S Inficon, Inc. · 1992
  • K911454FC2000S & S Inficon, Inc. · 1991
  • K902339Theraview Digital Portal Imaging ComputerS & S Inficon, Inc. · 1990

All 4 as S & S Inficon, Inc. →