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PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010472
510(k) Type
Traditional
Applicant
Thomson & Nielsen Electronics, Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/8/2001
Days to Decision
77 days
Submission Type
Summary

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010472
510(k) Type
Traditional
Applicant
Thomson & Nielsen Electronics, Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/8/2001
Days to Decision
77 days
Submission Type
Summary