FDA product code REQ: Laser Rangefinders, Time-Of-Flight Speed Measurement Products
REQ is the FDA product code for laser rangefinders, time-of-flight speed measurement products. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 3 recalls for REQ devices, 1 initiated in the last five years.
Definition
Product, laser, measures speed by time-of-flight. Includes laser range finders.
Classification
| Field | Value |
|---|---|
| Device name | Laser Rangefinders, Time-Of-Flight Speed Measurement Products |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for REQ devices
3 product recalls in 3 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2022-03-11.
| Year | Recalls |
|---|---|
| 2022 | 1 |
Frequently asked questions
What is FDA product code REQ?
REQ is the FDA product code for laser rangefinders, time-of-flight speed measurement products. It is a Not classified device, reviewed by the Unknown panel.
What device class is REQ?
Not classified.
Have REQ devices been recalled?
Yes: 3 product recalls across 3 recall events; the most recent began 2022-03-11.
Next steps
- Run an FDA pathway report with predicate devices for product code REQ
- Run a recall and safety report across every REQ manufacturer
- Watch product code REQ 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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