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FDA 510(k) Application Details - K960372
Device Classification Name
Clip, Aneurysm
More FDA Info for this Device
510(K) Number
K960372
Device Name
Clip, Aneurysm
Applicant
SCANLAN INTL., INC.
ONE SCANLAN PLAZA
ST PAUL, MN 55107 US
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Contact
KEN BLAKE
Other 510(k) Applications for this Contact
Regulation Number
882.5200
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Classification Product Code
HCH
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More FDA Info for this Product Code
Date Received
01/26/1996
Decision Date
04/26/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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