FDA product code QOJ: Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only)
QOJ is the FDA product code for apparatus, suction, operating-room, wall vacuum powered (export only). It is a Not classified device, reviewed by the General and Plastic Surgery panel. Devices under QOJ reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Intended to be used for the removal of prosthetic breast implant specimens.
Classification
| Field | Value |
|---|---|
| Device name | Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only) |
| Device class | Not classified |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for QOJ devices
openFDA lists no recalls for product code QOJ.
Frequently asked questions
What is FDA product code QOJ?
QOJ is the FDA product code for apparatus, suction, operating-room, wall vacuum powered (export only). It is a Not classified device, reviewed by the General and Plastic Surgery panel.
What device class is QOJ?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code QOJ
- Run a recall and safety report across every QOJ manufacturer
- Watch product code QOJ 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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