# K141199: Quentry Dose Review

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Jun 20, 2014 after 42 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K896095 (1990). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132763: Advanced Viewer, Brainlab AG (2014) Summary page 1.
- (no number) iPlan RT: named in the summary without a submission number

## Indications for use
Quentry Dose Review is a web based software for medical professionals that provides doctors, physicists and physicians with tools for secure online image (DICOM and DICOM RT) review including measurement and RT specific functions. such as display of dose distribution information, isodose lines, and dose volume histograms (DVH). It is not intended for the review of mammographic images, detailed treatment planning, plan approval or treatment of patients. It is also not intended to be used on mobile systems. For radiotherapy treatment plan approval, it is required to use the hospital specific workflows, tools and rccord&verify systems.

Source page: https://510kreport.com/device/K141199
Methodology: https://510kreport.com/methodology