DRZ — Oscillometer Class II

FDA Device Classification

FDA product code DRZ covers "Oscillometer", a Class II medical device regulated under 21 CFR 870.2675. Submissions are reviewed by the Cardiovascular panel.

Classification Details

Product Code
DRZ
Device Class
Class II
Regulation Number
870.2675
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No