LPCClass III

Device, Angioplasty, Laser, Coronary

Name: FDA product code LPC: Device, Angioplasty, Laser, Coronary
License: https://open.fda.gov/license/

Unknown

LPC is the FDA product code for Device, Angioplasty, Laser, Coronary, a class III device type. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code: LPC
Device name: Device, Angioplasty, Laser, Coronary
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 4

Companies listing this code with FDA

Companies whose registered establishments list this code

Spectranetics Corp.
Sterigenics U.S., LLC
Terumo BCT STERILIZATION SERVICES, Inc.