# K853753: Diamentor Patient X-Ray Exposure Indicator 07302

- Pathway: 510(k) (Traditional)
- Applicant: Victoreen, Inc.
- Decided: Oct 2, 1985 after 23 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K982319: Caregraph (1998), 10 descendants of its own
- K123097: Dose Tracking System Model Xidf-DTS801 (2013), 9 descendants of its own
- K132106: Infinix Angio Workstation W/DTS Software (2013), 8 descendants of its own
- K141541: Xidf-AWS801, Angio Workstation, V5.31 (2014), 7 descendants of its own
- K142736: XIDF-AWS801, Angio Workstation, v5.31 (2015), 6 descendants of its own

Source page: https://510kreport.com/device/K853753
Methodology: https://510kreport.com/methodology