# K003525: Voluson 730 Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Medison America, Inc.
- Decided: Nov 22, 2000 after 7 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.
1,255 later devices descend from it; 10 cite it directly.
6 of 1,256 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
- K022303: Philips M2424 Diagnostic Ultrasound System &Philips 21315 Diagnostic Ultrasound Transducer (2002), 1,155 descendants of its own
- K051139: Acuson Sequoia Diagnostic Ultrasound System (2005), 979 descendants of its own
- K052410: Acuson Sequoia Ultrasound System (2005), 972 descendants of its own
- K040060: Sonoline G50 and G60 S Diagnostic Ultrasound Systems (2004), 950 descendants of its own
- K043016: Sonoline Orchid Diagnostic Ultrasound System (2004), 927 descendants of its own

Source page: https://510kreport.com/device/K003525
Methodology: https://510kreport.com/methodology