FDA PMA FDA Class 3 Approved 🇺🇸 United States

Cardiac Ablation Percutaneous Catheter

PMA: P040036 · Supplement: S082 · Decision Sep 22, 2021
Classifications
1
FEI Numbers
52
Registration Numbers
52

Basic Information

Device Name
Cardiac Ablation Percutaneous Catheter
Trade Name
NAVISTAR THERMOCOOL, THERMOCOOL EZ STEER and THERMOCOOL SMARTTOUCH
PMA Number
P040036
Supplement Number
S082
Device Class
FDA Class 3
Product Code
LPB
Generic Name
Cardiac ablation percutaneous catheter
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
September 22, 2021
Date Received
May 17, 2021
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for updated labeling, including modified warnings and directions for use.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LPB Cardiac Ablation Percutaneous Catheter