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FDA 510(k) Application Details - K072900
Device Classification Name
More FDA Info for this Device
510(K) Number
K072900
Device Name
EXCELARREST FOAM
Applicant
HEMOSTASIS, LLC
5000 TOWNSHIP PARKWAY
ST. PAUL, MN 55110 US
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KEITH ROBERTS
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Regulation Number
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Classification Product Code
QSY
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Date Received
10/11/2007
Decision Date
10/26/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
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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