FDA 510(k) Applications Submitted by ELLIPSE A/S

FDA 510(k) Number Submission Date Device Name Applicant
K180406 02/14/2018 Ellipse Ydun Ellipse A/S
K140670 03/18/2014 ELLIPSE I2PL+/ELLIPSE MULTIFLEX+ ELLIPSE A/S
K150907 04/03/2015 Ellipse Nordlys/Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse Mjolner, Ellipse Nordlys Ultra Ellipse A/S
K161162 04/25/2016 Frax 1550 for Ellipse Nordlys/ Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse Mjolner, Ellipse Nordlys Ultra ELLIPSE A/S
K081408 05/19/2008 ELLIPSE MULTIFLEX ELLIPSE A/S
K072023 07/23/2007 ELLIPSE JUVIA, MODEL 9EJU7465 ELLIPSE A/S


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