FDA applicant

Chemetron Medical Products, Inc.

Mchenry, IL4 decisions1978–19790 recalls

FDA records 4 decisions for Chemetron Medical Products, Inc. (Mchenry, IL) from 1978 to 1979: 4 510(k) clearances. Most are in product codes CAX (Flowmeter, Tube, Thorpe, Back-Pressure…) and CAF (Nebulizer (Direct Patient Interface)). 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 Chemetron Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chemetron Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Chemetron Medical 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 “Chemetron”

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

Chemetron Health Systems 2 Chemetron Dental Products 1

Chemetron Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Chemetron”