# K954671: The Freedom Bed

- Pathway: 510(k) (Traditional)
- Applicant: Probed Medical Technologies, Inc.
- Decided: Apr 1, 1996 after 174 days
- Product code: IKZ (Bed, Patient Rotation, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5225
- 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 no predicate by number.

## Indications for use
The Freedom Bed PAR 3 is used to automatically reposition immobilized persons from side to side either manually or on a programmed schedule aide in the prevention of decubitus ulcers in bed ridden patients.

Source page: https://510kreport.com/device/K954671
Methodology: https://510kreport.com/methodology