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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name pump, infusion
510(k) Number K931318
Device Name 3400 INFUSION PUMP
Applicant
GRASEBY MEDICAL LTD.
COLONIAL WAY
WATFORD, HERTS.,  GB WD24 4LG
Applicant Contact WEYMAN
Correspondent
GRASEBY MEDICAL LTD.
COLONIAL WAY
WATFORD, HERTS.,  GB WD24 4LG
Correspondent Contact WEYMAN
Regulation Number880.5725
Classification Product Code
FRN  
Date Received03/16/1993
Decision Date 12/09/1994
Decision SE SUBJECT TO TRACKING REG (ST)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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