510(k) Report

FDA applicant

Scientific Imaging, Inc.

Woodstock, GA3 decisions1988–20050 recalls

FDA records 3 decisions for Scientific Imaging, Inc. (Woodstock, GA) from 1988 to 2005: 3 510(k) clearances. Most are in product codes JXE (Device, Nerve Conduction Velocity Measurement) and IYX (Camera, Scintillation (Gamma)). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Scientific Imaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Scientific Imaging, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Scientific Imaging, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • JXEDevice, Nerve Conduction Velocity Measurement1decision
  • IYXCamera, Scintillation (Gamma)1decision
  • IBJLight, Microscope1decision

What has FDA decided for it lately?

  • K052904Virtual Medical Systems Model VT3000Scientific Imaging, Inc. · 2005
  • K900773Nuclear MaxScientific Imaging, Inc. · 1990
  • K874750Video Analyzer 4000Scientific Imaging, Inc. · 1988

All 3 as Scientific Imaging, Inc. →