# K112502: Procedural Strecher with Intellidrive P8000

- Pathway: 510(k) (Traditional)
- Applicant: Hill-Rom Co.
- Decided: Sep 19, 2011 after 20 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
Longest line of descent: 2 generations back to K942948 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022309: Stryker Powered Wheeled Stretcher, Stryker Corp. (2002) Summary page 1.

## Indications for use
The Hill-Rom® Procedural Stretcher with Intellidrive® is intended to assist caregivers in the treatment and transportation of patients in all areas of hospitals, surgical centers, and other patient care facilities. The IntellidriveTM Transport System is permanently attached powered drive that is assembled into the existing Procedural Stretcher model. This feature lets the caregiver move the stretcher forward or reverse with very little applied force. The caregiver operates the system through the transport handles.

Source page: https://510kreport.com/device/K112502
Methodology: https://510kreport.com/methodology