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FDA 510(k) Application Details - K191629
Device Classification Name
Light Based Over The Counter Wrinkle Reduction
More FDA Info for this Device
510(K) Number
K191629
Device Name
Light Based Over The Counter Wrinkle Reduction
Applicant
iSMART Marketing Svcs Ltd
129 Green Lanes, Sutton Coldfield
Birmingham B735LT GB
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Contact
Susan D'Arcy
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
OHS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/19/2019
Decision Date
09/12/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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