GEMINI E
Manufactured by: ALLEN MEDICAL INSTRUMENTS CORP.

Proprietary Device Name:	GEMINI E
Common Generic Device Name:	ELECTRONIC STEHOSCOPE
Classification Name:	STETHOSCOPE, ELECTRONIC
FDA Regulation Number:	870.1875
Product Differentiation:
Product Website:

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