# K921297: Drager Dve 4000 Series System

- Pathway: 510(k) (Traditional)
- Applicant: Alm Surgical Equipment, Inc.
- Decided: Nov 27, 1992 after 255 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K961886: Drager Gemina Wall-Mounted Workplace (1996), 0 descendants of its own
- 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/K921297
Methodology: https://510kreport.com/methodology