FDA product code RHF: Digital Display Monitor
RHF is the FDA product code for digital display monitor. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 1 recall for RHF devices.
Definition
A monitor or projector that uses a high intensity light source to illuminate pixels to produce images driven from a digital image source.
Classification
| Field | Value |
|---|---|
| Device name | Digital Display Monitor |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RHF devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2008-09-09.
Frequently asked questions
What is FDA product code RHF?
RHF is the FDA product code for digital display monitor. It is a Not classified device, reviewed by the Unknown panel.
What device class is RHF?
Not classified.
Have RHF devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2008-09-09.
Next steps
- Run an FDA pathway report with predicate devices for product code RHF
- Run a recall and safety report across every RHF manufacturer
- Watch product code RHF 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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