510(k) Report

FDA applicant

Fraser Sweatman, Inc.

Mchenry, IL6 decisions1976–19770 recalls

FDA records 6 decisions for Fraser Sweatman, Inc. (Mchenry, IL) from 1976 to 1977: 6 510(k) clearances. Most are in product codes HSS (Halter, Head, Traction) and BZR (Mixer, Breathing Gases, Anesthesia Inhalation). 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, anesthesiology panel, where it files most

How often FDA has decided Fraser Sweatman, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fraser Sweatman, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fraser Sweatman, 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 “Fraser”

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