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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 K926243
Device Name ANGIOGRAPHIC CATHETER
Original Applicant
TARGET THERAPEUTICS
47201 lakeview blvd.
p.o. box 5120
freemont,  CA  94538
Original Contact grace carland
Regulation Number870.1200
Classification Product Code
DQO  
Date Received12/11/1992
Decision Date 08/16/1993
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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