FDA product code GOZ: Antisera, Fluorescent, B. Pertussis
GOZ is the FDA product code for antisera, fluorescent, b. pertussis. It is a Class I device, regulated under 21 CFR 866.3065 and reviewed by the Microbiology panel. Devices under GOZ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Antisera, Fluorescent, B. Pertussis |
| Device class | Class I |
| Regulation | 21 CFR 866.3065 |
| Review panel | MI — Microbiology |
| Medical specialty | Microbiology |
| Premarket route | 510(k) exempt |
Recalls for GOZ devices
openFDA lists no recalls for product code GOZ.
Frequently asked questions
What is FDA product code GOZ?
GOZ is the FDA product code for antisera, fluorescent, b. pertussis. It is a Class I device, regulated under 21 CFR 866.3065 and reviewed by the Microbiology panel.
What device class is GOZ?
Class I, regulation 21 CFR 866.3065. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code GOZ
- Run a recall and safety report across every GOZ manufacturer
- Watch product code GOZ 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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