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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 K870330
Device Name SP55 SYRINGE PUMP
Applicant
Vickers , Ltd.
Priestley Rd. Basingstoke
Hampshire
England,  GB RG249NP
Applicant Contact CANTRILL
Correspondent
Vickers , Ltd.
Priestley Rd. Basingstoke
Hampshire
England,  GB RG249NP
Correspondent Contact CANTRILL
Regulation Number880.5725
Classification Product Code
FRN  
Date Received01/28/1987
Decision Date 06/15/1987
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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