FDA 510(k) Application Details - K033268

Device Classification Name	Device, Acupressure   More FDA Info for this Device
510(K) Number	K033268
Device Name	Device, Acupressure
Applicant	SEA-BAND UK LTD. BUSINESS & TECH. CENTER BESSEMER DRIVE STEVENAGE, HERTS. SG1 2DX GB Other 510(k) Applications for this Company
Contact	NEIL R ARMSTRONG 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	10/09/2003
Decision Date	01/07/2004
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