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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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