# K944287: 7050 Ultrasound Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Biosound, Inc.
- Decided: Jun 2, 1995 after 273 days
- Product code: ITX (Transducer, Ultrasonic, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 892.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
184 later devices descend from it; 2 cite it directly.
2 of 185 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K981293: 7200 Ultrasound Imaging System (1998), 113 descendants of its own
- K020112: 50S Tringa Ultrasound Imaging System (2002), 112 descendants of its own
- K090505: Speq Ultrasound System (2009), 107 descendants of its own
- K102153: Mobius Ultrasound Imaging System (2011), 103 descendants of its own
- K133833: Nuvis Diagnostic Ultrasound System (2014), 87 descendants of its own

Source page: https://510kreport.com/device/K944287
Methodology: https://510kreport.com/methodology