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FDA 510(k) Application Details - K013082
Device Classification Name
Interferential Current Therapy
More FDA Info for this Device
510(K) Number
K013082
Device Name
Interferential Current Therapy
Applicant
MEDNET SERVICES, INC.
2855 ANTHONY LN. SOUTH, #B10
ST. ANTHONY, MN 55418 US
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Contact
DAVID L MATHEWS
Other 510(k) Applications for this Contact
Regulation Number
000.0000
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Classification Product Code
LIH
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More FDA Info for this Product Code
Date Received
09/14/2001
Decision Date
11/16/2001
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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