# K972115: Volker Hospital Bed, Model K960

- Pathway: 510(k) (Traditional)
- Applicant: Volker Healthcare, Inc.
- Decided: Aug 29, 1997 after 85 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
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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
This device is intended for medical purposes in hospitals or nursing homes for use by the staff or patients to adjust the height and surface contour of the bed using built-in electric motors. The device includes moveable and latchable side rails and wheels for movement of the bed to different locations. This bed is not intended for use on patients younger than 12 years of age.

Source page: https://510kreport.com/device/K972115
Methodology: https://510kreport.com/methodology