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DyeVert™ Plus Contrast Reduction System, DyeTect™ Contrast Monitoring System, DyeVert™ Plus EZ Contrast Reduction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190102
510(k) Type
Traditional
Applicant
Osprey Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2019
Days to Decision
268 days
Submission Type
Summary

DyeVert™ Plus Contrast Reduction System, DyeTect™ Contrast Monitoring System, DyeVert™ Plus EZ Contrast Reduction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190102
510(k) Type
Traditional
Applicant
Osprey Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2019
Days to Decision
268 days
Submission Type
Summary