# K923067: Sens-a-Ray

- Pathway: 510(k) (Traditional)
- Applicant: Regam Medical Systems
- Decided: Nov 27, 1992 after 155 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K024186: X-VIEW (2004), 0 descendants of its own
- K013176: Modification to: Sens-a-Ray System with Proimage Software (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K923067
Methodology: https://510kreport.com/methodology