FDA 510(k) Application Details - K000886

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K000886
Device Name	Catheter, Conduction, Anesthetic
Applicant	ABBOTT LABORATORIES D-389, AP-30 200 ABBOTT PARK ROAD ABBOTT PARK, IL 60064-3537 US Other 510(k) Applications for this Company
Contact	JILL N SACKETT Other 510(k) Applications for this Contact
Regulation Number	868.5120   More FDA Info for this Regulation Number
Classification Product Code	BSO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/2000
Decision Date	10/05/2000
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