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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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