FDA product code LIW: Fibrillator, Ac
LIW is the FDA product code for fibrillator, ac. It is a Unclassified device, reviewed by the Cardiovascular panel. Devices under LIW reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Fibrillator, Ac |
| Device class | Unclassified |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | 510(k) |
Recalls for LIW devices
openFDA lists no recalls for product code LIW.
Frequently asked questions
What is FDA product code LIW?
LIW is the FDA product code for fibrillator, ac. It is a Unclassified device, reviewed by the Cardiovascular panel.
What device class is LIW?
Unclassified. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code LIW
- Run a recall and safety report across every LIW manufacturer
- Watch product code LIW 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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