FDA 510(k) Applications Submitted by Elissa Burg

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130059	01/10/2013	ENDOFAST RELIANT SCP, ENDOFAST RELIANT LAP	IBI ISRAEL BIOMEDICAL INNOVATIONS LTD.
K220322	02/03/2022	Pollogen STOP U Model UXV Device	Pollogen Ltd.
K091389	05/11/2009	EQUALSHIELD LUER LOCK CONNECTOR PAIR	PLASTMED, LTD.
K151331	05/19/2015	The UltraPulse system (UltraPulse and UltraPulse DUO models,members of the modified Lumenis Family of UltraPulse SurgiTouch	LUMENIS LTD
K101940	07/12/2010	EQUASHIELD SYSTEM PROTECTIVE PLUS	EQUASHIELD MEDICAL LTD
K151947	07/15/2015	LightSheer Desire Light Laser System	LUMENIS LTD
K083152	10/24/2008	EQUASHIELD SYSTEM	PLASTMED, LTD.