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