FDA 510(k) Applications Submitted by ALAN CURTIS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020126	01/15/2002	MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)	SURX, INC.
K090306	02/06/2009	ARAGON SURGICAL RF SYSTEM L2 INSTRUMENT	ARAGON SURGICAL INC.
K070651	03/09/2007	ARAGON SURGICAL LAPCAP	ARAGON SURGICAL INC.
K070770	03/20/2007	GORE BALLOON SHEATH	W. L. GORE & ASSOCIATES, INC.
K110824	03/23/2011	ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENT	ARAGON SURGICAL INC.
K020952	03/25/2002	SURX RF SYSTEM	SURX, INC.
K011190	04/19/2001	SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM)	SURX, INC.
K081312	05/09/2008	ARAGON ONESHOT SYSTEM	ARAGON SURGICAL INC.
K081848	06/30/2008	LIPOSE FAT TRANSFER SYSTEM	LIPOSE CORP.
K093075	09/30/2009	ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT	ARAGON SURGICAL INC.
K073452	12/10/2007	MODIFICATION TO: ARAGON SURGICAL LAPCAP	ARAGON SURGICAL INC.