510(k) Report

FDA applicant

Beta Med Pharmaceuticals, Inc.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Beta Med Pharmaceuticals, Inc. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code KHE (Reagent, Occult Blood). 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 Beta Med Pharmaceuticals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beta Med Pharmaceuticals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KHEReagent, Occult Blood1decision

What has FDA decided for it lately?

  • K830919Occult-AlertBeta Med Pharmaceuticals, Inc. · 1983

The one decision as Beta Med Pharmaceuticals, Inc. →

Other applicant names beginning “Beta”

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

Beta Bionics, Inc. 9Beta Medical Products Co. 3Beta Biomed Services, Inc. 2Beta Labs, Inc. 1Beta Optical Co, Inc. 1Beta Toys, Inc. 1Beta Chemicals, Inc. 1Beta Healthcare Products Pvt., Ltd. 1