FDA 510(k) Application Details - K030937

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K030937
Device Name	Anesthesia Conduction Kit
Applicant	ARROW INTERNATIONAL, INC. 2400 BERNVILLE RD. READING, PA 19605-9607 US Other 510(k) Applications for this Company
Contact	BRANDON EPTING Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/2003
Decision Date	04/23/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review