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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 K964210
Device Name RETRIEVER II
Original Applicant
TARGET THERAPEUTICS
47201 lakeview blvd.
p.o. box 5120
freemont,  CA  94538
Original Contact laraine pangelina
Regulation Number870.1200
Classification Product Code
DQO  
Date Received10/22/1996
Decision Date 10/31/1997
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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