FDA 510(k) Application Details - K955298

Device Classification Name	Meter, Conductivity, Non-Remote   More FDA Info for this Device
510(K) Number	K955298
Device Name	Meter, Conductivity, Non-Remote
Applicant	AUTOMATA MEDICAL INSTRUMENTATION, INC. 7830 EAST REDFIELD RD., SUITE 12 SCOTTSDALE, AZ 85260 US Other 510(k) Applications for this Company
Contact	LINDA V MASANO Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FIZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/20/1995
Decision Date	02/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review