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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