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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 K932895
Device Name RIVER PUMP
Applicant
River Medical, Inc.
7737 Kenamar Ct.
San Diego,  CA  92121
Applicant Contact JIM C CAPUTO
Correspondent
River Medical, Inc.
7737 Kenamar Ct.
San Diego,  CA  92121
Correspondent Contact JIM C CAPUTO
Regulation Number880.5725
Classification Product Code
FRN  
Date Received06/14/1993
Decision Date 03/31/1994
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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