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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name mixture, hematology quality control
510(k) Number K013898
Device Name R&D RET-LINE KIT
Applicant
R & D SYSTEMS, INC.
614 MCKINLEY PL., N.E.
minneapolis,  MN  55413
Applicant Contact ralph e hogancamp
Correspondent
R & D SYSTEMS, INC.
614 MCKINLEY PL., N.E.
minneapolis,  MN  55413
Correspondent Contact ralph e hogancamp
Regulation Number864.8625
Classification Product Code
JPK  
Date Received11/23/2001
Decision Date 01/22/2002
Decision substantially equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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