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FDA 510(k) Applications Submitted by RICK ROSATI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140013
01/02/2014
SOPIX INSIDE, SOPIX2 INSIDE
SOPRO - ACTEON GROUP
K110379
02/10/2011
AIR-N-GO
SATELEC
K100410
02/16/2010
PIEZOELECTRIC SYSTEM
SATELEC
K131151
04/23/2013
ENDOCENTER
SATELEC-ACTEON GROUP
K091252
04/29/2009
IMPLANT CENTER 2
SATELEC
K091331
05/05/2009
PIEZOTOME 2
SATELEC
K121685
06/07/2012
SOPROCARE
SOPRO
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
K111978
07/12/2011
SULCUS BLUE
PRODUITS DENTAIRES PIERRE ROLLAND
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
K082116
07/28/2008
HEMOSTASYL PASTE
SATELEC
K112188
07/29/2011
PIEZOTOME SOLO
SATELEC - ACTEON, INC.
K092329
08/04/2009
SOPIX 2
SOPRO
K092583
08/21/2009
SOPROLIFE
SOPRO
K082796
09/23/2008
SOPRO 184 CAMERA
SOPRO
K113430
11/21/2011
PROULTRA PIEZO ULTRASONIC
SATELEC-ACTEON GROUP
K103813
12/29/2010
SOPRO 281
SOPRO
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