FDA applicant

Harvard Laboratories

Mchenry, IL8 decisions1980–19820 recalls

FDA records 8 decisions for Harvard Laboratories (Mchenry, IL) from 1980 to 1982: 8 510(k) clearances. Most are in product codes FPK (Tubing, Fluid Delivery) and CAE (Airway, Oropharyngeal, Anesthesiology). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Harvard Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Harvard”

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

Harvard Apparatus, Inc. 9 Harvard Medical Devices, Ltd. 5 Harvard Clinical Technology 2

Harvard Laboratories

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Harvard”