FDA applicant

Gri Medical Products, Inc.

Norwalk, CT1 decision1990–19900 recalls

FDA records 1 decision for Gri Medical Products, Inc. (Norwalk, CT) in 1990: 1 510(k) clearance. All are in product code DSF (Recorder, Paper Chart). 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, cardiovascular panel, where it files most

How often FDA has decided Gri Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Gri Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?