# K942055: Drager-Vapor 19.1

- Pathway: 510(k) (Traditional)
- Applicant: North American Grager
- Decided: Jan 27, 1995 after 274 days
- Product code: CAD (Vaporizer, Anesthesia, Non-Heated)
- Device class: 2
- Regulation: 21 CFR 868.5880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices 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.

## Most influential descendants
- K973051: Drager-Vapor 19.1 W/Plug System S Plus (1997), 1 descendant of its own
- K981773: Drager-Vapor 19.3 (1998), 0 descendants of its own
- K981472: Drager-Vapor 19.1 W/Plug System S Plus (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K942055
Methodology: https://510kreport.com/methodology