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FDA 510(k) Application Details - K060158
Device Classification Name
More FDA Info for this Device
510(K) Number
K060158
Device Name
NET-2000 MICROCURRENT STIMULATOR
Applicant
Auri-Stem Medical Inc.
4655 Kirkwood Court
Boulder, CO 80301 US
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Contact
LEWIS WARD
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Regulation Number
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Classification Product Code
QJQ
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Date Received
01/20/2006
Decision Date
10/13/2006
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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