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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 K760666
Device Name 4-WAY STOPCOCK W/LUER-LOCK FITTING
Applicant
AMERICAN VIGGO
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
AMERICAN VIGGO
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number880.5440
Classification Product Code
FMG  
Date Received09/17/1976
Decision Date 12/02/1976
Decision substantially equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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