FDA applicant

Cranbury Medical Labs, Inc.

Mchenry, IL7 decisions1982–19820 recalls

FDA records 7 decisions for Cranbury Medical Labs, Inc. (Mchenry, IL) in 1982: 7 510(k) clearances. All are in product code HGM (System, Monitoring, Perinatal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Cranbury Medical Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cranbury Medical Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cranbury Medical Labs, Inc.

Which product codes does it file in?

What has FDA decided for it lately?