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FDA 510(k)

NAOMI-CT

K-Number: K123332 · 2013-07-18

ApplicantLk Consulting Group
Decision Date2013-07-18
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NAOMI-CT is the device name listed in this FDA 510(k) record. The listed applicant is Lk Consulting Group. It received FDA 510(k) clearance on 2013-07-18 under 510(k) number K123332. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAOMI-CT?

NAOMI-CT is a medical device that received FDA 510(k) clearance on 2013-07-18. The listed applicant is Lk Consulting Group. The 510(k) number is K123332.

When did NAOMI-CT receive FDA 510(k) clearance?

NAOMI-CT received FDA 510(k) clearance on 2013-07-18, under 510(k) number K123332.

Who is the listed applicant for NAOMI-CT?

The FDA 510(k) record lists Lk Consulting Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAOMI-CT?

The FDA product code for NAOMI-CT is OAS.

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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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