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FDA 510(k) Application Details - K070217
Device Classification Name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
More FDA Info for this Device
510(K) Number
K070217
Device Name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Applicant
NEURO RESOURCE GROUP, INC.
1100 JUPITER RD., STE. 190
PLANO, TX 75074 US
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Contact
KRISTA OAKES
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Regulation Number
882.5890
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Classification Product Code
NFO
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More FDA Info for this Product Code
Date Received
01/23/2007
Decision Date
04/04/2008
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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