OMNI LIGHT
Manufactured by: AMERICAN MEDICAL BIOCARE INC.

Proprietary Device Name:	OMNI LIGHT
Common Generic Device Name:	INTENSE PULSED LIGHT SYSTEM
Classification Name:	LASER INSTRUMENT, SURGICAL, POWERED
FDA Regulation Number:	878.4810
Product Differentiation:
Product Website:

Copyright © 2000, 2001, 2002, 2003, 2004, 2005 - ZapConnect.com Medical Device Industry Portal
All Rights Reserved - Patent Pending
OCCDV5