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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, percutaneous
510(k) Number K003410
Device Name CONCENTRIC RETRIEVER, MODEL 90030
Original Applicant
CONCENTRIC MEDICAL, INC.
2585 leghorn st.
moutian view,  CA  94043
Original Contact sam lazzara
Regulation Number870.1250
Classification Product Code
DQY  
Date Received11/02/2000
Decision Date 05/22/2001
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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