FDA product code MFA: Device, Removal, Pacemaker Electrode, Percutaneous
MFA is the FDA product code for device, removal, pacemaker electrode, percutaneous. It is a Class III device, reviewed by the Cardiovascular panel. Devices under MFA reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Device, Removal, Pacemaker Electrode, Percutaneous |
| Device class | Class III |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MFA devices
openFDA lists no recalls for product code MFA.
Frequently asked questions
What is FDA product code MFA?
MFA is the FDA product code for device, removal, pacemaker electrode, percutaneous. It is a Class III device, reviewed by the Cardiovascular panel.
What device class is MFA?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MFA
- Run a recall and safety report across every MFA manufacturer
- Watch product code MFA for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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