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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 K002006
Device Name LIFESHIELD ADDITIVE PIERCING PIN
Original Applicant
ABBOTT LABORATORIES
dept. 389, ap30
200 abbott park rd.
abbott park,  IL  60064 -3537
Original Contact thomas p sampogna
Regulation Number880.5440
Classification Product Code
FPA  
Date Received07/03/2000
Decision Date 08/10/2000
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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