FDA product code POT: Lockbox (Export Only)
POT is the FDA product code for lockbox (export only). It is a Not classified device, reviewed by the General Hospital panel. Devices under POT reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
The lockbox is intended to hold an infusion pump and keep the medication syringe contained within the pump relatively secure.
Classification
| Field | Value |
|---|---|
| Device name | Lockbox (Export Only) |
| Device class | Not classified |
| Review panel | HO — General Hospital |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for POT devices
openFDA lists no recalls for product code POT.
Frequently asked questions
What is FDA product code POT?
POT is the FDA product code for lockbox (export only). It is a Not classified device, reviewed by the General Hospital panel.
What device class is POT?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code POT
- Run a recall and safety report across every POT manufacturer
- Watch product code POT 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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