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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 K933545
Device Name SIEMENS FLUID DELIVERY SYSTEM, MMT-9500
Applicant
Siemens Infusions Systems
12744 San Fernando Rd.
Sylmar,  CA  91342
Applicant Contact ROBERT W CALLAHAN
Correspondent
Siemens Infusions Systems
12744 San Fernando Rd.
Sylmar,  CA  91342
Correspondent Contact ROBERT W CALLAHAN
Regulation Number880.5725
Classification Product Code
FRN  
Date Received07/20/1993
Decision Date 09/29/1994
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
Predetermined Change
Control Plan Authorized		 No
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