# K942043: Drager Dve 8000/1/2 Series Syst W/Dve 4002 and 8032E

- Pathway: 510(k) (Traditional)
- Applicant: Alm Surgical Equipment, Inc.
- Decided: Jul 13, 1994 after 76 days
- Product code: FQO (Table, Operating-Room, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 878.4960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K961742: Drager Dve 8080/81/82 with Dve 4002 or Dve 4001 Series System (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K942043
Methodology: https://510kreport.com/methodology