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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, intravascular, diagnostic
510(k) Number K874815
Device Name TARGET THERAPEUTICS STERILE PRODUCTS
Original Applicant
TARGET THERAPEUTICS
2100 south sepulveda blvd.
los angeles,  CA  90025
Original Contact marie daniels
Regulation Number870.1200
Classification Product Code
DQO  
Date Received11/20/1987
Decision Date 02/05/1988
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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