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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 K051838
Device Name MODIFIED CONCENTRIC RETRIEVER, MODEL 90039
Original Applicant
CONCENTRIC MEDICAL, INC.
1380 shorebird way
mountain view,  CA  94043
Original Contact jean m caillouette
Regulation Number870.1250
Classification Product Code
DQY  
Date Received07/07/2005
Decision Date 09/01/2005
Decision substantially equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
summary summary
Type Special
Reviewed by Third Party No
Combination Product No
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