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OXYLOG 2000 PLUS SYSTEM (MODEL 5705080), OXYLOG 2000 PLUS BASIC DEVICE (MODEL 5705082)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082600
510(k) Type
Traditional
Applicant
Draeger Medical B.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
79 days
Submission Type
Summary

OXYLOG 2000 PLUS SYSTEM (MODEL 5705080), OXYLOG 2000 PLUS BASIC DEVICE (MODEL 5705082)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082600
510(k) Type
Traditional
Applicant
Draeger Medical B.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
79 days
Submission Type
Summary