FDA applicant

Mcgaw Laboratories

Mchenry, IL3 decisions1976–19780 recalls

FDA records 3 decisions for Mcgaw Laboratories (Mchenry, IL) from 1976 to 1978: 3 510(k) clearances. Most are in product codes KTZ (Caliper) and KNT (Tubes, Gastrointestinal (And Accessories)). 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, orthopedic panel, where it files most

How often FDA has decided Mcgaw Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcgaw Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mcgaw Laboratories’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 Respiratory Therapy 8

Mcgaw Laboratories

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mcgaw”