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FDA 510(k)

AIGIS-XO

K-Number: K024145 · 2003-03-07

ApplicantSb Lucius, Inc.
Decision Date2003-03-07
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIGIS-XO 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 2003-03-07 under 510(k) number K024145. 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 AIGIS-XO?

AIGIS-XO is a medical device that received FDA 510(k) clearance on 2003-03-07. The listed applicant is Sb Lucius, Inc.. The 510(k) number is K024145.

When did AIGIS-XO receive FDA 510(k) clearance?

AIGIS-XO received FDA 510(k) clearance on 2003-03-07, under 510(k) number K024145.

Who is the listed applicant for AIGIS-XO?

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 AIGIS-XO?

The FDA product code for AIGIS-XO is EJT.

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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-SOFTK024144AIGIS-PT

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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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