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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 K891176
Device Name INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)
Original Applicant
MULTI-MED, INC.
p.o. box 660
west swanzey,  NH  03469
Original Contact alan p reid
Regulation Number880.5440
Classification Product Code
FPA  
Date Received03/06/1989
Decision Date 05/18/1989
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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