FDA applicant

Thompson Respiration Products, Inc.

Mchenry, IL6 decisions1978–19820 recalls

FDA records 6 decisions for Thompson Respiration Products, Inc. (Mchenry, IL) from 1978 to 1982: 6 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and CAP (Monitor, Airway Pressure (Includes Gauge…). 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 Thompson Respiration Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thompson Respiration Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thompson Respiration Products, 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 “Thompson”

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

Thompson Surgical Instruments, Inc. 3 Thompson Mis, Inc. 1

Thompson Respiration Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Thompson”