# K000695: GE Dolphin Diagnostic Ultrasound System, Ultrasonic Pulsed Doppler Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Mar 16, 2000 after 15 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.
488 later devices descend from it; 1 cites it directly.
0 of 489 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
- K020789: GE Vivid 3 Expert; GE Vivid 3 Pro (2002), 487 descendants of its own
- K071985: GE Vivid S5 and S6 Diagnostic Ultrasound (2007), 412 descendants of its own
- K033139: GE Marlin Ultrasound (2003), 350 descendants of its own
- K061525: GE Vivid - I (2006), 349 descendants of its own
- K092079: Modification to GE Vivid S5 and S6 Diagnostic Ultrasound (2009), 331 descendants of its own

Source page: https://510kreport.com/device/K000695
Methodology: https://510kreport.com/methodology