OXYLOG 1000, MODEL 2M86840— 510(k) K010793

Substantially Equivalent

Drager Medizintechnik GmbH

FDA 510(k) clearance K010793 for OXYLOG 1000, MODEL 2M86840, Substantially Equivalent on 2001-12-20. Applicant: Drager Medizintechnik GmbH.

Clearance details

Applicant: Drager Medizintechnik GmbH
Product code: Code CBK
Advisory panel: Anesthesiology
Date received: 2001-03-16
Decision date: 2001-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Telford, PA, US

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Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.