FDA 510(k) Application Details - K973441

Device Classification Name	System, Radiation Therapy, Radionuclide   More FDA Info for this Device
510(K) Number	K973441
Device Name	System, Radiation Therapy, Radionuclide
Applicant	PATTERSON CONSULTING GROUP, INC. 18140 SMOKESIGNAL DR. SAN DIEGO, CA 92127 US Other 510(k) Applications for this Company
Contact	CAROL PATTERSON Other 510(k) Applications for this Contact
Regulation Number	892.5750   More FDA Info for this Regulation Number
Classification Product Code	IWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/1997
Decision Date	04/01/1998
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