FDA 510(k) Applications Submitted by STELLARTECH RESEARCH CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K041383	05/25/2004	STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 AND 1100C-230	STELLARTECH RESEARCH CORP.
K032721	09/03/2003	MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)	STELLARTECH RESEARCH CORP.
K050831	04/01/2005	STELLARTECH COAGULATION SYSTEM 2, MODELS 1100C-115A AND 1100C-230A	STELLARTECH RESEARCH CORP.
K040240	02/03/2004	STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)	STELLARTECH RESEARCH CORP.
K061544	06/05/2006	STELLARTECH 100 COAGULATION SYSTEM	STELLARTECH RESEARCH CORP.
K032062	07/03/2003	STELLARTECH COAGULATION SYSTEM, MODELS (1100C-115 & 1100C-230)	STELLARTECH RESEARCH CORP.
K032452	08/11/2003	MODIFICATION TO: STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 & 100C-230	STELLARTECH RESEARCH CORP.
K013139	09/19/2001	STELLARTECH COAGULATION SYSTEM	STELLARTECH RESEARCH CORP.
K042909	10/21/2004	STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230A	STELLARTECH RESEARCH CORP.
K023765	11/12/2002	STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)	STELLARTECH RESEARCH CORP.
K994173	12/10/1999	STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230	STELLARTECH RESEARCH CORP.