FDA applicant

Chroma Products, Inc.

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Chroma Products, Inc. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code KZL (Device, Warming. Blood And Plasma). 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 Chroma Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chroma Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Chroma”

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

Chroma Vision Medical Systems, Inc. 3

Chroma Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Chroma”