FDA 510(k) Application Details - K201272

Device Classification Name	System, Applicator, Radionuclide, Remote-Controlled   More FDA Info for this Device
510(K) Number	K201272
Device Name	System, Applicator, Radionuclide, Remote-Controlled
Applicant	Nucletron BV Waardgelder 1 Veenendaal 3905TH NL Other 510(k) Applications for this Company
Contact	Rigo Meens Other 510(k) Applications for this Contact
Regulation Number	892.5700   More FDA Info for this Regulation Number
Classification Product Code	JAQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/12/2020
Decision Date	07/16/2020
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