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FDA 510(k) Application Details - K093594
Device Classification Name
Cannula, Sinus
More FDA Info for this Device
510(K) Number
K093594
Device Name
Cannula, Sinus
Applicant
ACCLARENT, INC.
1525-B O'BRIEN DR.
MENLO PARK, CA 94025 US
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Contact
COURTNEY KALOF
Other 510(k) Applications for this Contact
Regulation Number
878.4800
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Classification Product Code
KAM
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More FDA Info for this Product Code
Date Received
11/19/2009
Decision Date
03/03/2010
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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