# K051861: The Savion Industries  Medi-Cruiser Model MS777

- Pathway: 510(k) (Traditional)
- Applicant: Savion Industries, Ltd.
- Decided: Sep 28, 2005 after 83 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.
No later device cites it as a predicate yet.
0 of 1 device 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) Hausted® POWERTRAN 1 M Series Stretcher: named in the summary without a submission number

## Indications for use
the device is a motorized device intended for medical purposes to assist in transfer of patient to and from beds, chairs, treatment facilities. wheelchairs or transport vehicles.

Source page: https://510kreport.com/device/K051861
Methodology: https://510kreport.com/methodology