FDA applicant
Bfi- Medical Waste Systems
FDA records 6 decisions for Bfi- Medical Waste Systems (Rolling Meadows, IL) from 1982 to 1998: 6 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and IYX (Camera, Scintillation (Gamma)). 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 Bfi- Medical Waste Systems’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bfi- Medical Waste Systems since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bfi- Medical Waste Systems’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) Report