# K964952: Veridose V (Five), Model Number 37-705

- Pathway: 510(k) (Traditional)
- Applicant: Victoreen, Inc.
- Decided: Jul 21, 1997 after 223 days
- Product code: JAD (System, Therapeutic, X-Ray)
- 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
Longest line of descent: 1 generation back to K912249 (1991). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K912249: Patient Dose Monitor, Theta Systems, Inc. (1991) Summary page 1.

## Indications for use
The Veridose V (Five) - Model Number 37-705 is used to provide integrated dose and dose rate readout capabilities for radiation sensing diodes when used for patient dose verification or quality assurance in radiation therapy.

Source page: https://510kreport.com/device/K964952
Methodology: https://510kreport.com/methodology