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FDA 510(k)

NEO 76

K-Number: K024141 · 2003-03-06

ApplicantSb Lucius, Inc.
Decision Date2003-03-06
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEO 76 is the device name listed in this FDA 510(k) record. The listed applicant is Sb Lucius, Inc.. It received FDA 510(k) clearance on 2003-03-06 under 510(k) number K024141. 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 NEO 76?

NEO 76 is a medical device that received FDA 510(k) clearance on 2003-03-06. The listed applicant is Sb Lucius, Inc.. The 510(k) number is K024141.

When did NEO 76 receive FDA 510(k) clearance?

NEO 76 received FDA 510(k) clearance on 2003-03-06, under 510(k) number K024141.

Who is the listed applicant for NEO 76?

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

What is the FDA product code for NEO 76?

The FDA product code for NEO 76 is EJT.

Other records listing Sb Lucius, 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.

K031010MIRACLE 98K024135AIGIS-PLUSK024143AIGIS-FINEK024142AIGIS-SUPERK024136AIGIS-SOFTK024145AIGIS-XO

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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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