# K950889: ADEL 5000

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Oct 16, 1995 after 230 days
- Product code: HDD (Table, Obstetrical, Ac-Powered (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.4900
- Recalls of this device: 4 (0 Class I)
- 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.

## Recalls of this device
- Mar 31, 2005 · Not classified · Z-0793-05: Trendelenburg and reverse trendelenburg features may not function.
- Jan 26, 2004 · Not classified · Z-0526-04: A potential shock hazard exists if the night light is damaged.
- Jan 26, 2004 · Not classified · Z-0524-04: A potential shock hazard exists if the night light is damaged.
- Jan 26, 2004 · Not classified · Z-0525-04: A potential shock hazard exists if the night light is damaged.

Source page: https://510kreport.com/device/K950889
Methodology: https://510kreport.com/methodology