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FDA 510(k)

NEUCODIA

K-Number: K081591 · 2009-05-15

ApplicantVerisci Corporation
Decision Date2009-05-15
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUCODIA is the device name listed in this FDA 510(k) record. The listed applicant is Verisci Corporation. It received FDA 510(k) clearance on 2009-05-15 under 510(k) number K081591. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUCODIA?

NEUCODIA is a medical device that received FDA 510(k) clearance on 2009-05-15. The listed applicant is Verisci Corporation. The 510(k) number is K081591.

When did NEUCODIA receive FDA 510(k) clearance?

NEUCODIA received FDA 510(k) clearance on 2009-05-15, under 510(k) number K081591.

Who is the listed applicant for NEUCODIA?

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

What is the FDA product code for NEUCODIA?

The FDA product code for NEUCODIA is GWE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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