FDA applicant

Midwest Analog & Digital, Inc.

Mchenry, IL3 decisions1978–19850 recalls

FDA records 3 decisions for Midwest Analog & Digital, Inc. (Mchenry, IL) from 1978 to 1985: 3 510(k) clearances. Most are in product codes DSF (Recorder, Paper Chart) 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 Midwest Analog & Digital, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest Analog & Digital, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Midwest”

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

Midwest 13 Midwest City Hearing Aid Center 12 Midwest Rf, LLC 9 Midwest Orthodontic Mfg. 7 Midwest Dental Products Corp. 5 Midwest Reprocessing Center, LLC 4 Midwest Metabolic Support Group 4 Midwest X-Ray Equipment Co. 3 Midwest Implant Sales, Inc. 3 Midwest Eye Laboratories, Inc. 2 Midwest Ophthalmic Instruments, Inc. 1 Midwest Marketing Service 1

Midwest Analog & Digital, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”