FDA 510(k) Applications Submitted by OLE KOFOD
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K180406 |
02/14/2018 |
Ellipse Ydun |
Ellipse A/S |
K060516 |
02/27/2006 |
ELLIPSE 12PL, MODEL 9ESL7228 |
DANISH DERMATOLOGIC DEVELOPMENT 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 |
K052688 |
09/28/2005 |
ELLIPSE FLEX PPT, MODEL 9ESF7255 |
DANISH DERMATOLOGIC DEVELOPMENT A/S |
K192951 |
10/21/2019 |
Ellipse Frax 1940 for Ellipse Nordlys and Ellipse Ydun |
Ellipse A/S |
K043255 |
11/24/2004 |
ELLIPSE LIGHT SPT |
DANISH DERMATOLOGIC DEVELOPMENT A/S |
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