# K041924: Hausted Powertran Series Stretcher

- Pathway: 510(k) (Traditional)
- Applicant: STERIS Corporation
- Decided: Sep 9, 2004 after 55 days
- Product code: INK (Stretcher, Wheeled, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Stryker ZOOM® Motorized Stretchers: named in the summary without a submission number
- (no number) Stryker Powered Wheeled Stretcher: named in the summary without a submission number

## Most influential descendants
- 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
- K172327: VMA™ System version 3.0 (2017), 7 descendants of its own

## Indications for use
The Hausted® POWERTRAN T M Series Stretcher is a powered patient transport. This device is a motorized device intended for medical purposes to assist in the transfer of patients to and from the bath, beds, chairs, treatment modalities, and transport vehicles. The FDA has classified powered patient transports as a Class II device.

Source page: https://510kreport.com/device/K041924
Methodology: https://510kreport.com/methodology