FDA 510(k) Application Details - K960185

Device Classification Name	Thermometer, Clinical Mercury   More FDA Info for this Device
510(K) Number	K960185
Device Name	Thermometer, Clinical Mercury
Applicant	AMSIA INTL., INC. 833 TOWNE CENTER DR. POMONA, CA 91767 US Other 510(k) Applications for this Company
Contact	RICHARD Y LI, PH.D. Other 510(k) Applications for this Contact
Regulation Number	880.2920   More FDA Info for this Regulation Number
Classification Product Code	FLK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/1996
Decision Date	03/28/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review