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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 K914067
Device Name RETRIEVAL DEVICE
Applicant
TARGET THERAPEUTICS
130 rio robles
p.o. box 610458
san jose,  CA  95134
Contact laura andeen
Regulation Number870.1200
Classification Product Code
DQO  
Date Received09/11/1991
Decision Date 12/10/1991
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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