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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 K911931
Device Name LUER LOCK INJECTION CAP
Applicant
Dmd Products
Post Office Box 2360
Nevada City,  CA  95959
Applicant Contact JOHN T WRIGHT
Correspondent
Dmd Products
Post Office Box 2360
Nevada City,  CA  95959
Correspondent Contact JOHN T WRIGHT
Regulation Number880.5440
Classification Product Code
FPA  
Date Received04/30/1991
Decision Date 06/18/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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