FDA applicant

Bissell Medical Products, Inc.

Naperville, IL6 decisions1985–19950 recalls

FDA records 6 decisions for Bissell Medical Products, Inc. (Naperville, IL) from 1985 to 1995: 6 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and FPP (Stretcher, Hand-Carried). 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 Bissell Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Bissell Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?