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FDA 510(k)

ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE

K-Number: K896540 · 1990-04-19

ApplicantNuclear Data Systems
Decision Date1990-04-19
Product CodeIZD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Data Systems. It received FDA 510(k) clearance on 1990-04-19 under 510(k) number K896540. 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 ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE?

ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is Nuclear Data Systems. The 510(k) number is K896540.

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

ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE received FDA 510(k) clearance on 1990-04-19, under 510(k) number K896540.

Who is the listed applicant for ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE?

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

What is the FDA product code for ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE?

The FDA product code for ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE 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 Systems 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.

K925650IMAGEVIEW 5000

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.

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