FDA applicant

Stanford Assoc., Inc.

Mchenry, IL2 decisions1979–19790 recalls

FDA records 2 decisions for Stanford Assoc., Inc. (Mchenry, IL) in 1979: 2 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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 Stanford Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stanford Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stanford Assoc., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Stanford”

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

Stanford Scientific, Inc. 4 Stanford Laboratories 2 Stanford Professional Products 2

Stanford Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stanford”