FDA product code REO: Analytical Measuring And Detection Laser Product
REO is the FDA product code for analytical measuring and detection laser product. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 1 recall for REO devices.
Definition
Product, laser, instrument, analyze/detect chemical species
Classification
| Field | Value |
|---|---|
| Device name | Analytical Measuring And Detection Laser Product |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for REO devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2011-04-27.
Frequently asked questions
What is FDA product code REO?
REO is the FDA product code for analytical measuring and detection laser product. It is a Not classified device, reviewed by the Unknown panel.
What device class is REO?
Not classified.
Have REO devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2011-04-27.
Next steps
- Run an FDA pathway report with predicate devices for product code REO
- Run a recall and safety report across every REO manufacturer
- Watch product code REO 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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