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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name set, administration, intravascular
510(k) Number K853327
Device Name JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION
Applicant
JUFREY MULTIMED CORP.
PATTON, BOGGS & BLOW
2550 M STREET NW
WASHINGTON,  DC  20037
Applicant Contact JRA FISHMAN
Correspondent
JUFREY MULTIMED CORP.
PATTON, BOGGS & BLOW
2550 M STREET NW
WASHINGTON,  DC  20037
Correspondent Contact JRA FISHMAN
Regulation Number880.5440
Classification Product Code
FPA  
Date Received08/08/1985
Decision Date 08/21/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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