FDA applicant

Automated Screening Devices

Mchenry, IL2 decisions1978–19800 recalls

FDA records 2 decisions for Automated Screening Devices (Mchenry, IL) from 1978 to 1980: 2 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). 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 Automated Screening Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automated Screening Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Automated”

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

Automated Medical Products Corp. 6 Automated IV Systems, Inc. 1 Automated Ophthalmics, Inc. 1 Automated Testing Services, Ltd. 1 Automated Lens System 1 Automated Imaging Diagnostics, LLC 1

Automated Screening Devices

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Automated”