510(k) Report

FDA applicant

David Bull Laboratories, USA, Inc.

Scottsdale, AZ2 decisions1991–19940 recalls

FDA records 2 decisions for David Bull Laboratories, USA, Inc. (Scottsdale, AZ) from 1991 to 1994: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and LHI (Set, I.V. Fluid Transfer). 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 David Bull Laboratories, USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for David Bull Laboratories, USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — David Bull Laboratories, USA, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like David Bull Laboratories, USA, 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 “David”

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