# K912249: Patient Dose Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Theta Systems, Inc.
- Decided: Aug 30, 1991 after 101 days
- Product code: KPZ (Generator, High Voltage, X-Ray, Therapeutic)
- Device class: 2
- Regulation: 21 CFR 892.5900
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K030175: 2 BASIC (2003), 0 descendants of its own
- K964952: Veridose V (Five), Model Number 37-705 (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K912249
Methodology: https://510kreport.com/methodology