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FDA 510(k) Applications Submitted by Venus Concept Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150161
01/23/2015
Venus Viva SR Device
Venus Concept Ltd.
K143554
12/15/2014
Venus Legacy CX
Venus Concept Ltd.
K152790
09/25/2015
Venus Versa System
VENUS CONCEPT LTD.
K162765
09/30/2016
Venus Velocity Diode Laser System
Venus Concept Ltd.
K153717
12/24/2015
Venus Versa System
Venus Concept Ltd.
K140629
03/11/2014
VENUS SWAN(MP)2
VENUS CONCEPT LTD.
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