RGUNot classified

X-Ray Field Indicator Light Field (Non-Laser)

Unknown

RGU is the FDA product code for X-Ray Field Indicator Light Field (Non-Laser). FDA's definition for this code reads: "A noncoherent light source incorporated in a diagnostic x-ray system that is irradiated onto the film screen area indicating the x-radiation area. The beam is usually scanned to show a rectangular region for patient placement". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: RGU
Device name: X-Ray Field Indicator Light Field (Non-Laser)
FDA definition: A noncoherent light source incorporated in a diagnostic x-ray system that is irradiated onto the film screen area indicating the x-radiation area. The beam is usually scanned to show a rectangular region for patient placement.
Device class: Not classified
Review panel: Unknown
Submission type: FDA code null
GMP exempt: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code RGU.

Recent clearances

Product code RGU

FDA records hold no clearances under product code RGU.

Recent recalls

Product code RGU

FDA records show no recalls under product code RGU.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)