# K121287: HT-Wedge

- Pathway: 510(k) (Traditional)
- Applicant: D.T. Davis Enterprises Ltd. T/A Hovertech Int'L
- Decided: Oct 3, 2012 after 156 days
- Product code: FNG (Lift, Patient, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 880.5500
- 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 K926411 (1993). 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)
- K041503: Hoverjack Air Patient Lift Device, D.T. Davis Enterprises, Ltd. (2004) Summary page 1.

## Indications for use
The purpose of the HT-Wedge is to pneumatically lift and position the head and chest of a patient who is lying in the supine position without manual lifting.

Source page: https://510kreport.com/device/K121287
Methodology: https://510kreport.com/methodology