Last synced on 9 May 2025 at 11:05 pm

DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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