# K942948: Stryker Powered Stretcher

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Jan 24, 1995 after 215 days
- Product code: FPO (Stretcher, Wheeled)
- Device class: 2
- Regulation: 21 CFR 880.6910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 2 cite it directly.
0 of 26 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
- K022309: Stryker Powered Wheeled Stretcher (2002), 20 descendants of its own
- K090136: Steris Cmax XLT Surgical Table (2009), 11 descendants of its own
- K112109: The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection Device (2011), 10 descendants of its own
- K130743: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion Normalizer Patient Handling and Data Coll (2013), 9 descendants of its own
- K133875: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion Normalizer Patient Handling and Data (2014), 8 descendants of its own

Source page: https://510kreport.com/device/K942948
Methodology: https://510kreport.com/methodology