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FDA 510(k) Application Details - K183189
Device Classification Name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
More FDA Info for this Device
510(K) Number
K183189
Device Name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Applicant
Micro Current Technology, Inc.
2244 1st Ave. South
Seattle, WA 98134 US
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Contact
David Suzuki
Other 510(k) Applications for this Contact
Regulation Number
882.5890
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Classification Product Code
NFO
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More FDA Info for this Product Code
Date Received
11/19/2018
Decision Date
04/17/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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