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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stopcock, I.V. Set
510(k) Number K955782
Device Name MED-NET STOPCOCKS
Applicant
Mednet, Inc.
10572 Mahoney Dr.
Sunland,  CA  91040
Applicant Contact ROBERT T MERICK
Correspondent
Mednet, Inc.
10572 Mahoney Dr.
Sunland,  CA  91040
Correspondent Contact ROBERT T MERICK
Regulation Number880.5440
Classification Product Code
FMG  
Date Received12/21/1995
Decision Date 02/21/1996
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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