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FDA 510(k) Application Details - K070766
Device Classification Name
Device, Acupressure
More FDA Info for this Device
510(K) Number
K070766
Device Name
Device, Acupressure
Applicant
PSI HEALTH SOLUTIONS, INC.
606 LIGHTHOUSE AVE. #168
PACIFIC GROVE, CA 93950 US
Other 510(k) Applications for this Company
Contact
ROMY TAORMINA
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
03/20/2007
Decision Date
07/26/2007
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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