# K961742: Drager Dve 8080/81/82 with Dve 4002 or Dve 4001 Series System

- Pathway: 510(k) (Traditional)
- Applicant: Alm Surgical Equipment, Inc.
- Decided: Jul 26, 1996 after 81 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
Longest line of descent: 1 generation back to K831086 (1983). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K921297: Drager Dve 4000 Series System, Alm Surgical Equipment, Inc. (1992) Summary page 1.
- K942043: Drager Dve 8000/1/2 Series Syst W/Dve 4002 and 8032E, Alm Surgical Equipment, Inc. (1994) Summary page 1.
- K831086: Ceiling Mounted Support, Amsco Co. (1983) Summary page 5.
- (no number) Heraeus Hanauport 810 Universal Ceiling Column: named in the summary without a submission number

## Indications for use
The Drager DVE 8080 System is a piece of durable equipment intended to provide ceiling mounted overhead physical support for anaesthesia machines, medical/surgical monitoring and related equipment, storage space, and ceiling mounted dispensing of medical gases and electrical power required in clinical settings, emergency rooms, intensive care, procedure rooms and operating rooms.

Source page: https://510kreport.com/device/K961742
Methodology: https://510kreport.com/methodology