510(k) Report

FDA applicant

Pattient Safety Innovations, Llp

Howell, MI1 decision2006–20060 recalls

FDA records 1 decision for Pattient Safety Innovations, Llp (Howell, MI) in 2006: 1 510(k) clearance. All are in product code ECX (Cylinder, Compressed Gas, And Valve). 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, anesthesiology panel, where it files most

How often FDA has decided Pattient Safety Innovations, Llp’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pattient Safety Innovations, Llp since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pattient Safety Innovations, Llp by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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