FDA product code JOA: Acid, Trifluoroacetic, Vitamin A, Hexane Extraction
JOA is the FDA product code for acid, trifluoroacetic, vitamin a, hexane extraction. It is a Class I device, regulated under 21 CFR 862.1805 and reviewed by the Clinical Chemistry panel. Devices under JOA reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Acid, Trifluoroacetic, Vitamin A, Hexane Extraction |
| Device class | Class I |
| Regulation | 21 CFR 862.1805 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Clinical Chemistry |
| Premarket route | 510(k) exempt |
Recalls for JOA devices
openFDA lists no recalls for product code JOA.
Frequently asked questions
What is FDA product code JOA?
JOA is the FDA product code for acid, trifluoroacetic, vitamin a, hexane extraction. It is a Class I device, regulated under 21 CFR 862.1805 and reviewed by the Clinical Chemistry panel.
What device class is JOA?
Class I, regulation 21 CFR 862.1805. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code JOA
- Run a recall and safety report across every JOA manufacturer
- Watch product code JOA 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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