FDA 510(k) Applications Submitted by BERTHOIN CLAUDE

FDA 510(k) Number Submission Date Device Name Applicant
K080220 01/29/2008 PIEZO ULTRASONIC DEVICE, MODEL ULTRASONIC BONE SURGERY; ULTRASONIC DEBRIDMENT DEVICE ITALIA MEDICA S.R.L.
K140380 02/14/2014 OPERA SWING GENERAL MEDICAL MERATE S.P.A.
K130442 02/21/2013 NEWTOM VGI AND NEWTOM 5G QR S.R.L.
K110840 03/25/2011 LIAC SORDINA S.P.A.
K081088 04/16/2008 MYRAY SKYVIEW CEFLA S.C.
K092917 09/22/2009 STERN'S S250 NORDAM CEFLA S.C.
K123381 11/01/2012 HYPERION X9 CEFLA S.C.
K133412 11/07/2013 S200, S300 CEFLA S.C.


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