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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name set, administration, intravascular
510(k) Number K960771
Device Name SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM
Applicant
RYMED TECHNOLOGIES, INC.
3110 BLUE SAGE DR.
WOODWARD,  OK  73801
Applicant Contact DANA W RYAN
Correspondent
RYMED TECHNOLOGIES, INC.
3110 BLUE SAGE DR.
WOODWARD,  OK  73801
Correspondent Contact DANA W RYAN
Regulation Number880.5440
Classification Product Code
FPA  
Date Received02/26/1996
Decision Date 12/10/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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