FDA product code RGW: Uv/Ir Research
RGW is the FDA product code for uv/ir research. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 1 recall for RGW devices.
Definition
A noncoherent ultraviolet or infrared light source used in research.
Classification
| Field | Value |
|---|---|
| Device name | Uv/Ir Research |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RGW devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2018-05-29.
| Year | Recalls |
|---|---|
| 2018 | 1 |
Frequently asked questions
What is FDA product code RGW?
RGW is the FDA product code for uv/ir research. It is a Not classified device, reviewed by the Unknown panel.
What device class is RGW?
Not classified.
Have RGW devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2018-05-29.
Next steps
- Run an FDA pathway report with predicate devices for product code RGW
- Run a recall and safety report across every RGW manufacturer
- Watch product code RGW 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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