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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 K925091
Device Name IVAC SYRING PUMP MODEL 770
Applicant
Y
10300 Campus Pt. Dr.
San Diego,  CA  92121
Applicant Contact JENNIFER S HANKARD
Correspondent
Y
10300 Campus Pt. Dr.
San Diego,  CA  92121
Correspondent Contact JENNIFER S HANKARD
Regulation Number880.5725
Classification Product Code
FRN  
Date Received10/07/1992
Decision Date 07/08/1993
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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