510(k) Report

FDA applicant

Swartz Medical Equipment

Mchenry, IL6 decisions1977–19770 recalls

FDA records 6 decisions for Swartz Medical Equipment (Mchenry, IL) in 1977: 6 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and DXQ (Blood Pressure Cuff). 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 Swartz Medical Equipment’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Swartz Medical Equipment since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Swartz Medical Equipment’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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