Last synced on 16 May 2025 at 11:05 pm

DyeVert™ NG Contrast Reduction System, DyeVert™ PLUS EZ Contrast Reduction System, DyeTect™ Contrast Monitoring Disposable Kit, Smart Syringe, 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
K183267
510(k) Type
Special
Applicant
Osprey Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
27 days
Submission Type
Summary

DyeVert™ NG Contrast Reduction System, DyeVert™ PLUS EZ Contrast Reduction System, DyeTect™ Contrast Monitoring Disposable Kit, Smart Syringe, 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
K183267
510(k) Type
Special
Applicant
Osprey Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
27 days
Submission Type
Summary