# K092939: Patlog 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Oncolog Medical QA AB
- Decided: Oct 9, 2009 after 15 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: 2 generations back to K950061 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090044: Patlog, Patlog Patient Handling System, Patlog Toplog Table Top, Model (S) 1.0, 1.0, C, Oncolog Medical QA AB (2009) Summary page 1.
- K950061: Hercules Radiation Therapy Couch, Precision Therapy Intl., Inc. (1995) Summary page 1.

## Indications for use
System for patient positioning and fixation on the treatment couch, including transportation of the patient from preparation site and/or diagnostic surveys to the treatment unit Intended User The PatLog Patient Handling System is intended to be used by qualified radiotherapy personnel trained in using the device.

Source page: https://510kreport.com/device/K092939
Methodology: https://510kreport.com/methodology