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FDA 510(k) Application Details - K092780
Device Classification Name
Interferential Current Therapy
More FDA Info for this Device
510(K) Number
K092780
Device Name
Interferential Current Therapy
Applicant
FUJI DYNAMICS LIMITED
23/F., UNIT 1-3,
788 CHEUNG SHA WAN ROAD
KOWLOON, HONG KONG CN
Other 510(k) Applications for this Company
Contact
CHING KONG LEE
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LIH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/10/2009
Decision Date
01/07/2010
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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