# K964515: Acclaim Series QD6000,QD6001,QD6002 and Series QD3000,QD3001, QD3002

- Pathway: 510(k) (Traditional)
- Applicant: M.C. Healthcare Products, Inc.
- Decided: Dec 31, 1996 after 76 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K964515
Methodology: https://510kreport.com/methodology