510(k) Report

FDA applicant

Pacific Consolidated Industries

Orange, CA6 decisions1990–20111 recall

FDA records 6 decisions for Pacific Consolidated Industries (Orange, CA) from 1990 to 2011: 6 510(k) clearances. All are in product code CAW (Generator, Oxygen, Portable). Its devices cite 9 predicates, 5 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Pacific Consolidated Industries Llp”, “Pacific Consolidated Industries, LLC”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Pacific Consolidated Industries’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007: 12011: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

Planning a device like Pacific Consolidated Industries’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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