FDA 510(k) Application Details - K102460

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K102460
Device Name	Catheter, Conduction, Anesthetic
Applicant	SUMMIT MEDICAL PRODUCTS, INC 2480 SOUTH MAIN STREET SALT LAKE CITY, UT 84115 US Other 510(k) Applications for this Company
Contact	MARKO VAN AMEN 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	08/27/2010
Decision Date	01/13/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review