510(k) Report

FDA applicant

Matheson Gas Products, Inc.

East Rutheford, NJ5 decisions1987–19880 recalls

FDA records 5 decisions for Matheson Gas Products, Inc. (East Rutheford, NJ) from 1987 to 1988: 5 510(k) clearances. Most are in product codes BXK (Gas, Calibration (Specified Concentration)) and GEX (Powered Laser Surgical Instrument). 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 Matheson Gas Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Matheson Gas Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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