FDA applicant

Mcgaw Respiratory Therapy

Mchenry, IL8 decisions1976–19770 recalls

FDA records 8 decisions for Mcgaw Respiratory Therapy (Mchenry, IL) from 1976 to 1977: 8 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and CBD (Bottle, Collection, Breathing System…). 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 Mcgaw Respiratory Therapy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcgaw Respiratory Therapy since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mcgaw Respiratory Therapy’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 “Mcgaw”

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

Mcgaw, Inc. 13 Mcgaw Laboratories 3

Mcgaw Respiratory Therapy

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mcgaw”