# K945400: Hitachi Dynamic 3D Imaging System,SF-VA100

- Pathway: 510(k) (Traditional)
- Applicant: Hitachi Medical Corp. of America
- Decided: Nov 20, 1995 after 382 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K964990: Hitachi SX-VA30 C-Arm Fluoroscopic/Angiographic System (SX-VA30) (1997), 1 descendant of its own
- K991231: Hitachi Versiflex (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K945400
Methodology: https://510kreport.com/methodology