FDA 510(k) Application Details - K093139

Device Classification Name	Catheter, Angioplasty, Peripheral, Transluminal   More FDA Info for this Device
510(K) Number	K093139
Device Name	Catheter, Angioplasty, Peripheral, Transluminal
Applicant	CLEAR STREAM TECHNOLOGIES, LTD. MOYNE UPPER, ENNISCORTHY ENNISCORTHY IE Other 510(k) Applications for this Company
Contact	FIONA NI MHULLAIN Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	LIT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/05/2009
Decision Date	12/30/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review