510(k) Report

FDA applicant

Barco NV Barcoview

Albuquerque, NM14 decisions2004–20040 recalls

FDA records 14 decisions for Barco NV Barcoview (Albuquerque, NM) in 2004: 14 510(k) clearances. All are in product code LLZ (System, Image Processing, Radiological). Its devices cite 15 predicates, 2 of them its own earlier devices. 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, radiology panel, where it files most

How often FDA has decided Barco NV Barcoview’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Barco NV Barcoview since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Barco NV Barcoview by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Barco NV Barcoview’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 “Barco”

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