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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Injector And Syringe, Angiographic
510(k) Number K171217
Device Name DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System
Applicant
Osprey Medical, Inc.
5600 Rowland Rd. Suite 250
Minnetonka,  MN  55343
Applicant Contact Melanie Hess
Correspondent
Osprey Medical, Inc.
5600 Rowland Rd. Suite 250
Minnetonka,  MN  55343
Correspondent Contact Melanie Hess
Regulation Number870.1650
Classification Product Code
DXT  
Date Received04/26/2017
Decision Date 05/26/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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