FDA 510(k) Applications Submitted by SCOTT KARLER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070129	01/16/2007	SONOTIP II ULTRASOUND NEEDLE SYSTEM	MEDI-GLOBE CORPORATION
K010549	02/26/2001	BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)	MEDI-GLOBE CORP.
K011261	04/25/2001	STONE EXTRACTOR BALLOON CATHETER	MEDI-GLOBE CORP.
K091257	04/29/2009	MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM	MEDI-GLOBE CORPORATION
K061222	05/02/2006	INJECTRA INJECTION NEEDLE	MEDI-GLOBE CORP.
K051247	05/16/2005	SONOTIP II ULTRASOUND NEEDLE SYSTEM	MEDI-GLOBE CORP.
K061684	06/15/2006	MEDI-GLOBE ROTA-CUT SPHINCTEROTOME	MEDI-GLOBE CORPORATION
K142258	08/14/2014	PolyCatch Retrieval Device	Medi-Globe Corporation
K153264	11/12/2015	EasyPass Guidewire	MEDI-GLOBE CORPORATION
K133763	12/11/2013	SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM	MEDI-GLOBE CORPORATION
K083802	12/22/2008	SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025	MEDI-GLOBE CORPORATION