FDA 510(k) Application Details - K963992

Device Classification Name	Electrode, Ion-Specific, Chloride   More FDA Info for this Device
510(K) Number	K963992
Device Name	Electrode, Ion-Specific, Chloride
Applicant	MEDICA CORP. 14 DEANGELO DR. BEDFORD, MA 01730 US Other 510(k) Applications for this Company
Contact	Photios Makris Other 510(k) Applications for this Contact
Regulation Number	862.1170   More FDA Info for this Regulation Number
Classification Product Code	CGZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/04/1996
Decision Date	11/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review