FDA applicant

Hazleton Dutchland, Inc.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Hazleton Dutchland, Inc. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code GRC (Antigen, Cf (Including Cf Control), Mumps Virus). 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, microbiology panel, where it files most

How often FDA has decided Hazleton Dutchland, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hazleton Dutchland, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hazleton Dutchland, Inc.’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 “Hazleton”

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

Hazleton Research Products, Inc. 47

Hazleton Dutchland, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hazleton”