510(k) Report

FDA applicant

Cardinal Scale Mfg. Co.

Webb City, MO1 decision1993–19930 recalls

FDA records 1 decision for Cardinal Scale Mfg. Co. (Webb City, MO) in 1993: 1 510(k) clearance. All are in product code FRW (Scale, Patient). 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, general hospital panel, where it files most

How often FDA has decided Cardinal Scale Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cardinal Scale Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FRWScale, Patient1decision

What has FDA decided for it lately?

  • K924847Detecto Model 6700 SeriesCardinal Scale Mfg. Co. · 1993

The one decision as Cardinal Scale Mfg. Co. →

Other applicant names beginning “Cardinal”

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

Cardinal Health, Inc. 28Cardinal Health200, LLC 26Cardinal Health, Alaris Products 9Cardinal Health-Medical Products and Services 6Cardinal Health 207, Inc. 5Cardinal Spine, LLC 4Cardinal Health 200, Inc. 4Cardinal Health 303,Inc. 4Cardinal Health Germany 234 GmbH 2