FDA applicant
David Bull Laboratories, USA, Inc.
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
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.
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.
See the 510(k) ReportOther applicant names beginning “David”
FDA records each applicant name separately; these may or may not be the same firm.