FDA 510(k) Application Details - K983125

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K983125
Device Name	Anesthesia Conduction Kit
Applicant	RUSCH INTL. TALL PINES PARK JAFFREY, NH 03452 US Other 510(k) Applications for this Company
Contact	JAMES R WHITNEY 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	09/08/1998
Decision Date	11/17/1998
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