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FDA 510(k) Application Details - K073386
Device Classification Name
Stimulator, Electrical, Transcutaneous, For Arthritis
More FDA Info for this Device
510(K) Number
K073386
Device Name
Stimulator, Electrical, Transcutaneous, For Arthritis
Applicant
PAIN MANAGEMENT TECHNOLOGIES
1340 HOME AVE. , BLDG A
AKRON, OH 44310 US
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Contact
JOSHUA LEFKOVITZ
Other 510(k) Applications for this Contact
Regulation Number
882.5890
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Classification Product Code
NYN
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More FDA Info for this Product Code
Date Received
12/03/2007
Decision Date
07/30/2008
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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