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IHJ — Blender, Sputum Class I

FDA Device Classification

FDA product code IHJ covers "Blender, Sputum", a Class I medical device regulated under 21 CFR 864.3010. Submissions are reviewed by the Pathology panel.

Classification Details

Product Code: IHJ
Device Class: Class I
Regulation Number: 864.3010
Submission Type
Review Panel: PA
Medical Specialty: Pathology
Implant: No