FDA 510(k) Application Details - K992992

Device Classification Name	System, Tomography, Computed, Emission   More FDA Info for this Device
510(K) Number	K992992
Device Name	System, Tomography, Computed, Emission
Applicant	TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 TUSTIN, CA 92781-2068 US Other 510(k) Applications for this Company
Contact	DIANA THORSON Other 510(k) Applications for this Contact
Regulation Number	892.1200   More FDA Info for this Regulation Number
Classification Product Code	KPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/07/1999
Decision Date	12/03/1999
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