FDA 510(k) Application Details - K001095

Device Classification Name	Analyzer, Gas, Oxygen, Gaseous-Phase   More FDA Info for this Device
510(K) Number	K001095
Device Name	Analyzer, Gas, Oxygen, Gaseous-Phase
Applicant	TELEDYNE ANALYTICAL INSTRUMENTS 16830 CHESTNUT ST. CITY OF INDUSTRY, CA 91749 US Other 510(k) Applications for this Company
Contact	RAY KHAJAVI Other 510(k) Applications for this Contact
Regulation Number	868.1720   More FDA Info for this Regulation Number
Classification Product Code	CCL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/04/2000
Decision Date	06/30/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review