FDA applicant

Hazleton Research Products, Inc.

Denver, PA47 decisions1985–19860 recalls

FDA records 47 decisions for Hazleton Research Products, Inc. (Denver, PA) from 1985 to 1986: 47 510(k) clearances. Most are in product codes KIT (Media And Components, Synthetic Cell And…) and KIS (Sera, Animal And Human). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Hazleton Research Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hazleton Research Products, 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 Dutchland, Inc. 1

Hazleton Research Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hazleton”