FDA applicant

Raco Products Co.

Cleveland, OH4 decisions1992–19940 recalls

FDA records 4 decisions for Raco Products Co. (Cleveland, OH) from 1992 to 1994: 4 510(k) clearances. Most are in product codes DXH (Transmitters And Receivers…) and LDD (Dc-Defibrillator, Low-Energy, (Including…). 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 Raco Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Raco Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Raco Products Co.

Which product codes does it file in?

What has FDA decided for it lately?