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FDA 510(k) Applications Submitted by STEVE SALESKY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070102
01/10/2007
SOPRO 162 CAMERA
SOPRO
K080122
01/17/2008
SOPRO 670 ARTHROSCOPIC PUMP
SOPRO
K060274
02/02/2006
PIEZOTOME
SATELEC
K060275
02/02/2006
PIEZOTOME
SATELEC
K070783
03/21/2007
SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR
SOPRO
K071424
05/23/2007
PMAX NEWTRON XS
SATELEC-ACTEON GROUP
K071965
07/16/2007
I-SURGE
SATELEC
K072030
07/24/2007
IMPLANT CENTER
SATELEC-ACTEON GROUP
K072181
08/06/2007
MINI LED AUTOFOCUS
SATELEC
K042787
10/06/2004
IS 40 MICROMOTOR
SATELEC
K072912
10/12/2007
SOPRO 225 DUAL HALOGEN LIGHT SOURCE
SOPRO
K053328
12/01/2005
BIOSPLINT SPLINTING RIBBON
SATELEC
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