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DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System

Page Type
Cleared 510(K)
510(k) Number
K171217
510(k) Type
Special
Applicant
Osprey Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2017
Days to Decision
30 days
Submission Type
Summary

DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System

Page Type
Cleared 510(K)
510(k) Number
K171217
510(k) Type
Special
Applicant
Osprey Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2017
Days to Decision
30 days
Submission Type
Summary