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FDA 510(k) Application Details - K053509
Device Classification Name
Device, Acupressure
More FDA Info for this Device
510(K) Number
K053509
Device Name
Device, Acupressure
Applicant
ACUBAND INC.
101 LITTLE SILVER POINT ROAD
LITTLE SILVER, NJ 07739 US
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Contact
RICHARD GRIFFITH
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
MVV
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/16/2005
Decision Date
08/16/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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