510(k) Report

FDA applicant

Diagnostic Information, Inc.

Mchenry, IL3 decisions1976–19800 recalls

FDA records 3 decisions for Diagnostic Information, Inc. (Mchenry, IL) from 1976 to 1980: 3 510(k) clearances. All are in product code 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 Diagnostic Information, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diagnostic Information, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diagnostic Information, 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-Intensified3decisions

What has FDA decided for it lately?

  • K801166Pet-Scope II Model Dis-1611Diagnostic Information, Inc. · 1980
  • K771485Pet-TV X-Ray Image Intensifier SystemDiagnostic Information, Inc. · 1977
  • K761285Pet-ScopeDiagnostic Information, Inc. · 1976

All 3 as Diagnostic Information, Inc. →

Other applicant names beginning “Diagnostic”

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

Diagnostic Products Corp. 324Diagnostic Systems Laboratories, Inc. 94Diagnostic Chemicals, Ltd. (Usa) 77Diagnostic Reagents, Inc. 66Diagnostic Chemicals, Ltd. 66Diagnostic Hybrids, Inc. 37Diagnostic Technology, Inc. 28Diagnostic Solutions, Inc. 26Diagnostic Ultrasound Corp. 16Diagnostic Systems 14Diagnostic Reagent Tech. 10Diagnostic Specialties 8