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 | Device Class | Medical Specialty |
|---|---|---|---|
| LPB | Cardiac Ablation Percutaneous Catheter | FDA class 3 | Unknown |