FDA product code JGI: Atomic Absorption, Magnesium
JGI is the FDA product code for atomic absorption, magnesium. It is a Class I device, regulated under 21 CFR 862.1495 and reviewed by the Clinical Chemistry panel. Devices under JGI reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Atomic Absorption, Magnesium |
| Device class | Class I |
| Regulation | 21 CFR 862.1495 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Clinical Chemistry |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for JGI devices
openFDA lists no recalls for product code JGI.
Frequently asked questions
What is FDA product code JGI?
JGI is the FDA product code for atomic absorption, magnesium. It is a Class I device, regulated under 21 CFR 862.1495 and reviewed by the Clinical Chemistry panel.
What device class is JGI?
Class I, regulation 21 CFR 862.1495. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code JGI
- Run a recall and safety report across every JGI manufacturer
- Watch product code JGI 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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