# K945293: Top Acom Station

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jan 5, 1995 after 66 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K992073: AX Workstation (1999), 0 descendants of its own

## Recalls of this device
- Jun 16, 2004 · Not classified · Z-1477-04: possible problem reviewing images on the ACOM.M

Source page: https://510kreport.com/device/K945293
Methodology: https://510kreport.com/methodology