# K933202: Venus Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Jun 27, 1994 after 361 days
- Product code: IYN (System, Imaging, Pulsed Doppler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1,018 later devices descend from it; 2 cite it directly.
3 of 1,019 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
- K970901: GE Logiq 500 Diagnostic Ultrasound System (1997), 1,017 descendants of its own
- K991611: GE Logiq 500 (1999), 1,015 descendants of its own
- K040502: Sonoline Ebisu Diagnostic Ultrasound Systems (2004), 930 descendants of its own
- K042833: Sonoline G20 Diagnostic Ultrasound Systems (2004), 928 descendants of its own
- K043016: Sonoline Orchid Diagnostic Ultrasound System (2004), 927 descendants of its own

Source page: https://510kreport.com/device/K933202
Methodology: https://510kreport.com/methodology