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)

ND62T THYROID UPTAKE SYSTEM

K-Number: K841440 · 1984-06-05

ApplicantNuclear Data, Inc.
Decision Date1984-06-05
Product CodeIZD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ND62T THYROID UPTAKE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Data, Inc.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841440. The device is classified under product code IZD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND62T THYROID UPTAKE SYSTEM?

ND62T THYROID UPTAKE SYSTEM is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Nuclear Data, Inc.. The 510(k) number is K841440.

When did ND62T THYROID UPTAKE SYSTEM receive FDA 510(k) clearance?

ND62T THYROID UPTAKE SYSTEM received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841440.

Who is the listed applicant for ND62T THYROID UPTAKE SYSTEM?

The FDA 510(k) record lists Nuclear Data, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ND62T THYROID UPTAKE SYSTEM?

The FDA product code for ND62T THYROID UPTAKE SYSTEM is IZD.

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 Nuclear Data, Inc. 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.

K891466ACCUSPEC THYROID UPTAKE SYSTEMK881383ND1100 BONE DENSITY SCANNERK844835ND2100 SPINE SCANNERK844766ND1100 BONE DENSITY SCANNERK843349ND3100 VIDEO IMAGERK841352ND1200 RIA COUNTER

View all 7 devices →

Related Devices (Code: IZD)

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.

K123917DECLIPSESPECT VIEWERSurgiceye GmbHK101887CONFIDENT SURGERY SUITE 300, MODEL CSS300Surgiceye GmbHK013751HANDHELD GAMMA FINDER (HGF)Silicon Instruments GmhbK983768MODIFICATION TO GAMMA GUIDANCE SYSTEMRadiation Monitoring Devices, Inc.K982442C-TRAK AUTOMATIC ANALYZER (NAME CHANGE FROM ONCOPROBE II TO C-TRAK)Care Wise Medical Products Corp.K971167NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESNeoprobe Corp.

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.

↑