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FDA 510(k)

LUCIUS 76

K-Number: K023196 · 2002-11-01

ApplicantSb Lucius, Inc.
Decision Date2002-11-01
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LUCIUS 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 2002-11-01 under 510(k) number K023196. 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 LUCIUS 76?

LUCIUS 76 is a medical device that received FDA 510(k) clearance on 2002-11-01. The listed applicant is Sb Lucius, Inc.. The 510(k) number is K023196.

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

LUCIUS 76 received FDA 510(k) clearance on 2002-11-01, under 510(k) number K023196.

Who is the listed applicant for LUCIUS 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 LUCIUS 76?

The FDA product code for LUCIUS 76 is EJT.

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Other records listing Sb Lucius, Inc. as applicant

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Related Devices (Code: EJT)

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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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