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FDA 510(k)

GAMMACELL 3000 ELAN

K-Number: K952291 · 1995-08-25

ApplicantNordion International, Inc.
Decision Date1995-08-25
Product CodeMOT
DecisionSubstantially Equivalent

Device Summary

GAMMACELL 3000 ELAN is the device name listed in this FDA 510(k) record. The listed applicant is Nordion International, Inc.. It received FDA 510(k) clearance on 1995-08-25 under 510(k) number K952291. The device is classified under product code MOT. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAMMACELL 3000 ELAN?

GAMMACELL 3000 ELAN is a medical device that received FDA 510(k) clearance on 1995-08-25. The listed applicant is Nordion International, Inc.. The 510(k) number is K952291.

When did GAMMACELL 3000 ELAN receive FDA 510(k) clearance?

GAMMACELL 3000 ELAN received FDA 510(k) clearance on 1995-08-25, under 510(k) number K952291.

Who is the listed applicant for GAMMACELL 3000 ELAN?

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

What is the FDA product code for GAMMACELL 3000 ELAN?

The FDA product code for GAMMACELL 3000 ELAN is MOT.

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 Nordion International, 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.

K963497GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0

Related Devices (Code: MOT)

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.

K201177RadGil2R3 X-Ray L.L.CK181737Raycell MK1Best Theratronics LimitedK172087SANGRAYHitachi , Ltd.K161324Raycell Mk2Best Theratronics LimitedK082921RAD SOURCE X-RAY BLOOD IRRADIATOR, MODEL RS-3400Rad Source Technologies, Inc.K051065RAYCELL X-RAY BLOOD IRRADIATORMds Nordion

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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