FDA product code RDZ: Low-Power Laser Light Show Projector
RDZ is the FDA product code for low-power laser light show projector. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 1 recall for RDZ devices.
Definition
Product, laser, demo, projector, laser light show/display, class iiia/3r and lower; Laser projection system that incorporates a laser having a maximum radiation output of less than 5mw.
Classification
| Field | Value |
|---|---|
| Device name | Low-Power Laser Light Show Projector |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RDZ devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2017-11-21.
| Year | Recalls |
|---|---|
| 2017 | 1 |
Frequently asked questions
What is FDA product code RDZ?
RDZ is the FDA product code for low-power laser light show projector. It is a Not classified device, reviewed by the Unknown panel.
What device class is RDZ?
Not classified.
Have RDZ devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2017-11-21.
Next steps
- Run an FDA pathway report with predicate devices for product code RDZ
- Run a recall and safety report across every RDZ manufacturer
- Watch product code RDZ 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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