FDA product code RBS: Industrial X-Ray
RBS is the FDA product code for industrial x-ray. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 3 recalls for RBS devices.
Definition
An x-ray system used for industrial purposes to which the cabinet x-ray performance standard does not apply (21 cfr 1020.40).
Classification
| Field | Value |
|---|---|
| Device name | Industrial X-Ray |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RBS devices
3 product recalls in 3 recall events; 0 initiated in the last five years and 1 still open. Most recent: 2015-06-09.
Frequently asked questions
What is FDA product code RBS?
RBS is the FDA product code for industrial x-ray. It is a Not classified device, reviewed by the Unknown panel.
What device class is RBS?
Not classified.
Have RBS devices been recalled?
Yes: 3 product recalls across 3 recall events; the most recent began 2015-06-09.
Next steps
- Run an FDA pathway report with predicate devices for product code RBS
- Run a recall and safety report across every RBS manufacturer
- Watch product code RBS 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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