510(k) Report

FDA applicant

Biometric Analysis Group, Inc.

Mchenry, IL2 decisions1980–19800 recalls

FDA records 2 decisions for Biometric Analysis Group, Inc. (Mchenry, IL) in 1980: 2 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and DSI (Detector And Alarm, Arrhythmia). 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, cardiovascular panel, where it files most

How often FDA has decided Biometric Analysis Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biometric Analysis Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Biometric Analysis Group, 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?

  • DXGComputer, Diagnostic, Pre-Programmed, Single-Function1decision
  • DSIDetector And Alarm, Arrhythmia1decision

What has FDA decided for it lately?

  • K802472Biometric Erg SystemBiometric Analysis Group, Inc. · 1980
  • K802198Biometric Systolic Time Interval SystemBiometric Analysis Group, Inc. · 1980

All 2 as Biometric Analysis Group, Inc. →

Other applicant names beginning “Biometric”

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

Biometric Products, Inc. 5Biometric Research Institute, Inc. 2