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QMG — Shockwave Intravascular Lithotripsy System Class III

FDA Device Classification

FDA product code QMG covers "Shockwave Intravascular Lithotripsy System", a Class III medical device. Submissions are reviewed by the Unknown panel.

Classification Details

Product Code: QMG
Device Class: Class III
Regulation Number
Submission Type
Review Panel: CV
Medical Specialty: Unknown
Implant: No

Definition

Dilatation of coronary arteries prior to stenting