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

FDA 510(k) Number	Submission Date	Device Name	Applicant
K233922	12/13/2023	SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG	SATELEC-ACTEON GROUP
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