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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