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FDA 510(k)

CERANUM 87

K-Number: K021947 · 2002-08-26

ApplicantLucius Metals Com.
Decision Date2002-08-26
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERANUM 87 is the device name listed in this FDA 510(k) record. The listed applicant is Lucius Metals Com.. It received FDA 510(k) clearance on 2002-08-26 under 510(k) number K021947. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERANUM 87?

CERANUM 87 is a medical device that received FDA 510(k) clearance on 2002-08-26. The listed applicant is Lucius Metals Com.. The 510(k) number is K021947.

When did CERANUM 87 receive FDA 510(k) clearance?

CERANUM 87 received FDA 510(k) clearance on 2002-08-26, under 510(k) number K021947.

Who is the listed applicant for CERANUM 87?

The FDA 510(k) record lists Lucius Metals Com. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERANUM 87?

The FDA product code for CERANUM 87 is EJT.

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 Lucius Metals Com. 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.

K021948LUCIUS 62

Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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