FDA 510(k) Applications Submitted by BRUCE COREN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K091285	05/01/2009	AL T LASER, MODEL AVI HPLL-12	AVICENNA LASER TECHNOLOGY, INC.
K121363	05/07/2012	DIOWAVE LOW LEVEL COLD LASER SYSTEM	TECHNOLOGICAL MEDICAL ADVANCMENTS, INC. (TMA)
K031612	05/22/2003	ALT LASER, MODEL VTR 75	AVICENNA LASER TECHNOLOGY, INC.