# K974296: Model 720 Series Full/Semi Electric Bed 1120 Full Electric Bed

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Jan 6, 1998 after 50 days
- Product code: FNL (Bed, Ac-Powered Adjustable Hospital)
- Device class: 2
- Regulation: 21 CFR 880.5100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K925534 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925534: Full/Semi Electric Home Care Bed, Ivacare Corp. (1993) Summary page 1.

## Indications for use
To provide added comfort during periods of bedrest by permitting the user to adjust the surface contour of the bed to various positions.

Source page: https://510kreport.com/device/K974296
Methodology: https://510kreport.com/methodology