# K965010: Target 2 Version 1.1

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Jul 23, 1997 after 219 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 K896353 (1989). 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)
- K896353: GE Target Series 2, GE Medical Systems (1989) Summary page 2.

## Indications for use
The Target 2 V1.1 is a radiation oncology treatment planning system which uses CT and non-CT data to produce External Beam and Irregular Field plans, and non-CT data to provide Interstitial/Intracavitary Dosimetry plans.

Source page: https://510kreport.com/device/K965010
Methodology: https://510kreport.com/methodology