FDA applicant

Unitron Corp.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Unitron Corp. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code CBT (Arterial Blood Sampling Kit). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Unitron Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Unitron”

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

Unitron Industries, Inc. 69 Unitron Hearing 1

Unitron Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Unitron”