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FDA 510(k)

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50

K-Number: K010472 · 2001-05-08

ApplicantThomson & Nielsen Electronics, Ltd.
Decision Date2001-05-08
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 is the device name listed in this FDA 510(k) record. The listed applicant is Thomson & Nielsen Electronics, Ltd.. It received FDA 510(k) clearance on 2001-05-08 under 510(k) number K010472. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50?

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 is a medical device that received FDA 510(k) clearance on 2001-05-08. The listed applicant is Thomson & Nielsen Electronics, Ltd.. The 510(k) number is K010472.

When did PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 receive FDA 510(k) clearance?

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 received FDA 510(k) clearance on 2001-05-08, under 510(k) number K010472.

Who is the listed applicant for PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50?

The FDA 510(k) record lists Thomson & Nielsen Electronics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50?

The FDA product code for PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50 is IYE.

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Other records listing Thomson & Nielsen Electronics, Ltd. as applicant

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Related Devices (Code: IYE)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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