FDA 510(k) Applications Submitted by THOMSON & NIELSEN ELECTRONICS, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K010472 02/20/2001 PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 THOMSON & NIELSEN ELECTRONICS, LTD.
K041557 06/10/2004 MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W THOMSON & NIELSEN ELECTRONICS, LTD.
K032725 09/03/2003 MOSFET AUTOSENSE WIRELESS THOMSON & NIELSEN ELECTRONICS, LTD.
K013279 10/02/2001 MOSFET AUTOSENSE, MODEL TN-RD-60 THOMSON & NIELSEN ELECTRONICS, LTD.


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