# K893689: Vision Integrated Performance Option

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jul 20, 1989 after 65 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K965179: Insight Diagnostic Imaging Workstation Nit-DU0-Zoo (1997), 10 descendants of its own
- K982535: Insight Diagnostic Imaging Workstation (1998), 9 descendants of its own
- K990241: Accuimage, Accuview Diagnostic Imaging, Workstation W/Accuscore, Accuanalyze, Accuscope, Accushade, Accuvrt, and Accumip (1999), 8 descendants of its own
- K063221: Medweb Advanced 3D Web Pacs (2006), 1 descendant of its own
- K024149: Primelung (2003), 1 descendant of its own

Source page: https://510kreport.com/device/K893689
Methodology: https://510kreport.com/methodology