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FDA 510(k)

VITASCORE

K-Number: K072014 · 2007-11-08

ApplicantVitascore B.V.
Decision Date2007-11-08
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITASCORE is the device name listed in this FDA 510(k) record. The listed applicant is Vitascore B.V.. It received FDA 510(k) clearance on 2007-11-08 under 510(k) number K072014. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITASCORE?

VITASCORE is a medical device that received FDA 510(k) clearance on 2007-11-08. The listed applicant is Vitascore B.V.. The 510(k) number is K072014.

When did VITASCORE receive FDA 510(k) clearance?

VITASCORE received FDA 510(k) clearance on 2007-11-08, under 510(k) number K072014.

Who is the listed applicant for VITASCORE?

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

What is the FDA product code for VITASCORE?

The FDA product code for VITASCORE is MNR.

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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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