# K963705: Color Enhancement Function for the Ssa-380A

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: Dec 2, 1996 after 77 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
Longest line of descent: 1 generation back to K933743 (1994). 1 ancestor in all.
403 later devices descend from it; 2 cite it directly.
3 of 405 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K933743: SSA-380A, Toshiba America Medical Systems, In.C (1994) Summary page 1.

## Most influential descendants
- K991858: Ssa-390A/Power Vision 8000 (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
- K032281: Ssa-770A - Version 4, Aplio Diagnostic Ultrasound System (2003), 209 descendants of its own
- K063130: Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0 (2006), 205 descendants of its own

Source page: https://510kreport.com/device/K963705
Methodology: https://510kreport.com/methodology