# K984577: Drager Oxylog 2000

- Pathway: 510(k) (Special)
- Applicant: Drager, Inc.
- Decided: Jan 22, 1999 after 30 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
21 later devices descend from it; 3 cite it directly.
11 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Oxylog 2000: named in the summary without a submission number

## Most influential descendants
- K062267: Oxylog 3000 (2006), 20 descendants of its own
- K112006: Hamilton-TC1 (2012), 13 descendants of its own
- K120670: Hamilton-T1 (2012), 11 descendants of its own
- K121225: Hamilton-C2 (2012), 8 descendants of its own
- K123637: Hamilton-C3 (2012), 4 descendants of its own

## Indications for use
The Oxylog 2000 is a time cycled, volume constant transport and emergency ventilator for patients with tidal volumes starting at 100 mL. With applications in: mobile emergency and primary care of emergency patients patient transports in emergency rescue vehicles or by helicopter patient transfers by road or air inner hospital transport of ventilated patients emergency room secondary transports between hospitals

Source page: https://510kreport.com/device/K984577
Methodology: https://510kreport.com/methodology