FDA 510(k) Application Details - K041818

Device Classification Name	Transducer, Ultrasonic, Diagnostic   More FDA Info for this Device
510(K) Number	K041818
Device Name	Transducer, Ultrasonic, Diagnostic
Applicant	BOSTON SCIENTIFIC CORP. 47900 BAYSIDE PARKWAY FREMONT, CA 94538-6515 US Other 510(k) Applications for this Company
Contact	ROBERT Z PHILLIPS Other 510(k) Applications for this Contact
Regulation Number	892.1570   More FDA Info for this Regulation Number
Classification Product Code	ITX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/06/2004
Decision Date	11/10/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review