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FDA 510(k) Application Details - K090026
Device Classification Name
More FDA Info for this Device
510(K) Number
K090026
Device Name
CHITOGAUZE, MODELS 130, 131, 263, 264, 265, 266
Applicant
HEMCON MEDICAL TECHNOLOGIES, INC.
10575 SW CASCADE AVENUE
SUITE 130
PORTLAND, OR 97223-4363 US
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Contact
KEVIN HAWKINS
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Regulation Number
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Classification Product Code
QSY
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Date Received
01/05/2009
Decision Date
03/31/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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