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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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