Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W

K-Number: K041557 · 2004-06-25

ApplicantThomson & Nielsen Electronics, Ltd.
Decision Date2004-06-25
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W 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 2004-06-25 under 510(k) number K041557. 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 MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W?

MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W is a medical device that received FDA 510(k) clearance on 2004-06-25. The listed applicant is Thomson & Nielsen Electronics, Ltd.. The 510(k) number is K041557.

When did MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W receive FDA 510(k) clearance?

MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W received FDA 510(k) clearance on 2004-06-25, under 510(k) number K041557.

Who is the listed applicant for MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W?

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 MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W?

The FDA product code for MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W is IYE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K032725MOSFET AUTOSENSE WIRELESSK013279MOSFET AUTOSENSE, MODEL TN-RD-60K010472PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50

Related Devices (Code: IYE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

Official Source

View on FDA Database →

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

↑