# K141230: Doselab Pro

- Pathway: 510(k) (Traditional)
- Applicant: Mobius Medical Systems, LP
- Decided: Aug 27, 2014 after 106 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- 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 K935928 (1994). 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)
- K935928: Rit 113 Film Analysis System, Radiological Imaging Technology, Inc. (1994) Summary page 4.

## Indications for use
DoseLab Pro is quality assurance software intended to be used as part of a dosimetry verification system for linear accelerators. It can be used to import radiation-exposed images from scanned film, other measurement devices, and treatment planning systems to display differences between measured and calculated dose distributions.

Source page: https://510kreport.com/device/K141230
Methodology: https://510kreport.com/methodology