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MODIFICATION TO VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT/OXIMETRY MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082308
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2008
Days to Decision
118 days
Submission Type
Summary

MODIFICATION TO VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT/OXIMETRY MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082308
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2008
Days to Decision
118 days
Submission Type
Summary