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Business · 07/07/2003Updated: 10/17/2026 · 1 min read

FDA Classifies Breath Nitric Oxide Test System as Class II Device

Summary

The FDA has classified the breath nitric oxide test system as a Class II device, requiring special controls to ensure its safety and effectiveness, following a petition submitted under various medical device amendments.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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