FDA 510(k) Application Details - K001940

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K001940
Device Name	Anesthesia Conduction Kit
Applicant	MICOR, INC. 2855 OXFORD BLVD. ALLISON PARK, PA 15101 US Other 510(k) Applications for this Company
Contact	JEREMIAH COSTELLO 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	06/26/2000
Decision Date	08/11/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review