FDA 510(k) Application Details - K992660

Device Classification Name	More FDA Info for this Device
510(K) Number	K992660
Device Name	URF DIGITAL - OT
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH ISELIN, NJ 08830 US Other 510(k) Applications for this Company
Contact	MALGORZATA STANEK Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/1999
Decision Date	11/05/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review