FDA applicant

Dowit Service Co., Inc.

Montville, NJ2 decisions1988–19880 recalls

FDA records 2 decisions for Dowit Service Co., Inc. (Montville, NJ) in 1988: 2 510(k) clearances. Most are in product codes FCP (Box, Battery, Pocket) and MHX (Monitor, Physiological, Patient (With…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Dowit Service Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dowit Service Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dowit Service Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?