FDA 510(k) Applications Submitted by RALPH JUGO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050027	01/06/2005	LAPAROCISION SCOPE CONTROLLER SYSTEM	GMP/COMPANIES, INC.
K030795	03/12/2003	LIFESYNE SYSTEMS	GMP/COMPANIES, INC.
K071120	04/20/2007	AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999	AEMED, INC.