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FDA 510(k) Application Details - K022420
Device Classification Name
Device, Neurovascular Embolization
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510(K) Number
K022420
Device Name
Device, Neurovascular Embolization
Applicant
MICRUS CORP.
495 CLYDE AVE.
MOUNTAIN VIEW, CA 94043 US
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Contact
MARGARET WEBBER
Other 510(k) Applications for this Contact
Regulation Number
882.5950
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Classification Product Code
HCG
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More FDA Info for this Product Code
Date Received
07/24/2002
Decision Date
10/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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