FDA 510(k) Application Details - K002023

Device Classification Name	Campylobacter Pylori   More FDA Info for this Device
510(K) Number	K002023
Device Name	Campylobacter Pylori
Applicant	MEDMIRA LABORATORIES, INC. 155 CHAIN LAKE DR. HALIFAX, N.S. B3S 1B3 CA Other 510(k) Applications for this Company
Contact	TODD BISHOP Other 510(k) Applications for this Contact
Regulation Number	866.3110   More FDA Info for this Regulation Number
Classification Product Code	LYR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/03/2000
Decision Date	11/13/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review