510(k) Report

FDA applicant

Bill Dude Hospital Disposables, Inc.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Bill Dude Hospital Disposables, Inc. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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 Bill Dude Hospital Disposables, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bill Dude Hospital Disposables, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bill Dude Hospital Disposables, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bill Dude Hospital Disposables, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Bill”

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