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QFD — Tens For Sinus Pain Class II

FDA Device Classification

FDA product code QFD covers "Tens For Sinus Pain", a Class II medical device regulated under 21 CFR 882.5890. Submissions are reviewed by the Neurology panel.

Classification Details

Product Code: QFD
Device Class: Class II
Regulation Number: 882.5890
Submission Type
Review Panel: NE
Medical Specialty: Neurology
Implant: No

Definition

Electrical stimulation to relieve pain