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FDA 510(k) Application Details - K183692
Device Classification Name
Interferential Current Therapy
More FDA Info for this Device
510(K) Number
K183692
Device Name
Interferential Current Therapy
Applicant
Vision Quest Industries Inc./ dba VQ OrthoCare
1390 Decision Street, Suite A
Vista, CA 92081 US
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Contact
Mohamed Ouerghi
Other 510(k) Applications for this Contact
Regulation Number
000.0000
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Classification Product Code
LIH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/31/2018
Decision Date
06/12/2019
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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