FDA 510(k) Application Details - K973176

Device Classification Name	Cylinder, Gas (Empty)   More FDA Info for this Device
510(K) Number	K973176
Device Name	Cylinder, Gas (Empty)
Applicant	LOTUS TECHNOLOGIES 1215 RED RIVER ST. AUSTIN, TX 78701 US Other 510(k) Applications for this Company
Contact	DILIP J KARNIK Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	KGA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/25/1997
Decision Date	11/21/1997
Decision	SESK - SUBST EQUIV - KIT
Classification Advisory Committee	-
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review