FDA 510(k) Applications Submitted by SATELEC-ACTEON GROUP

FDA 510(k) Number Submission Date Device Name Applicant
K131151 04/23/2013 ENDOCENTER SATELEC-ACTEON GROUP
K111623 06/10/2011 I-ENDO DUAL SATELEC-ACTEON GROUP
K131906 06/26/2013 SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE SATELEC-ACTEON GROUP
K131997 06/28/2013 NEWTRON BOOSTER SATELEC-ACTEON GROUP
K132267 07/22/2013 NEWTRON P5, NEWTRON P5 B.LED SATELEC-ACTEON GROUP
K132322 07/25/2013 NEWTRON P5 XS B.LED SATELEC-ACTEON GROUP
K113430 11/21/2011 PROULTRA PIEZO ULTRASONIC SATELEC-ACTEON GROUP
K071424 05/23/2007 PMAX NEWTRON XS SATELEC-ACTEON GROUP
K072030 07/24/2007 IMPLANT CENTER SATELEC-ACTEON GROUP


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