LPB — Cardiac Ablation Percutaneous Catheter Class III

FDA Device Classification

FDA product code LPB covers "Cardiac Ablation Percutaneous Catheter", a Class III medical device. Submissions are reviewed by the Unknown panel.

Classification Details

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

Definition

This product code pertains to cardiac ablation catheters indicated for general indications, treatment of supraventricular tachycardia (svt) and ventricular tachycardia (vt). This product code excludes ablation catheters indicated for treatment of atrial flutter [product code oad] and atrial fibrillation [product code oae].