FDA 510(k) Application Details - K943824

Device Classification Name	Analyzer, Gas, Oxygen, Gaseous-Phase   More FDA Info for this Device
510(K) Number	K943824
Device Name	Analyzer, Gas, Oxygen, Gaseous-Phase
Applicant	AMETEK, INC. 300 WILLIAM PITT WAY PITTSBURGH, PA 15238 US Other 510(k) Applications for this Company
Contact	JOE VELTRY 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	05/02/1994
Decision Date	11/01/1996
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