# K930768: Orion Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Mar 15, 1994 after 392 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
221 later devices descend from it; 6 cite it directly.
0 of 222 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K964617: GE Logiq 700 Diagnostic Ultrasound System (1997), 217 descendants of its own
- K990248: Dicom Image Manager, Model 3-D Visualization Option (1999), 213 descendants of its own
- K992886: Powerview Ultrasound Workstation, Uidm-400A (1999), 212 descendants of its own
- K013633: Ssa-770A, Aplio Ultrasound System (2001), 211 descendants of its own
- K022400: Ssa-700A, Aplio Diagnostic Ultrasound System (2002), 210 descendants of its own

Source page: https://510kreport.com/device/K930768
Methodology: https://510kreport.com/methodology