510(k) Report

FDA applicant

Instrumentation Camera, Inc.

Mchenry, IL2 decisions1980–19810 recalls

FDA records 2 decisions for Instrumentation Camera, Inc. (Mchenry, IL) from 1980 to 1981: 2 510(k) clearances. Most are in product codes JAA (System, X-Ray, Fluoroscopic, Image-Intensified) and IZJ (Camera, X-Ray, Fluorographic, Cine Or Spot). 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 Instrumentation Camera, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Instrumentation Camera, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Instrumentation Camera, 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?

  • JAASystem, X-Ray, Fluoroscopic, Image-Intensified1decision
  • IZJCamera, X-Ray, Fluorographic, Cine Or Spot1decision

What has FDA decided for it lately?

  • K810716X-Ray Image Intensifier ProductsInstrumentation Camera, Inc. · 1981
  • K802132105MM Spot Film CameraInstrumentation Camera, Inc. · 1980

All 2 as Instrumentation Camera, Inc. →

Other applicant names beginning “Instrumentation”

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

Instrumentation Laboratory CO 327Instrumentation Industries, Inc. 46Instrumentation Laboratory (IL) Co. 5Instrumentation Specialties, Inc. 2