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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 K830389
Device Name ACCU-RYNGE PUMP SP-250
Applicant
Delta Medical Industries
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Delta Medical Industries
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number880.5725
Classification Product Code
FRN  
Date Received02/10/1983
Decision Date 09/12/1983
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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