FDA 510(k) Application Details - K011493

Device Classification Name	Calibrator, Dose, Radionuclide   More FDA Info for this Device
510(K) Number	K011493
Device Name	Calibrator, Dose, Radionuclide
Applicant	MENTOR CORP. 9727 VALLEY VIEW RD. EDEN PRAIRIE, MN 55344 US Other 510(k) Applications for this Company
Contact	GEORGE HOEDEMAN Other 510(k) Applications for this Contact
Regulation Number	892.1360   More FDA Info for this Regulation Number
Classification Product Code	KPT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/15/2001
Decision Date	10/01/2002
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