FDA 510(k) Application Details - K101768

Device Classification Name	System, Tomography, Computed, Emission   More FDA Info for this Device
510(K) Number	K101768
Device Name	System, Tomography, Computed, Emission
Applicant	MIE GMBH HAUPTSTR. 112 SETH D-23845 DE Other 510(k) Applications for this Company
Contact	THOMAS KUHL 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	06/23/2010
Decision Date	10/05/2010
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