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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 K925813
Device Name DIAGNOSTIC INTRAVASCULAR CATHETER
Applicant
TARGET THERAPEUTICS
47201 lakeview blvd.
p.o. box 5120
freemont,  CA  94538
Contact laraine pangelina
Regulation Number870.1200
Classification Product Code
DQO  
Date Received11/17/1992
Decision Date 03/23/1994
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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