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FDA 510(k)

DERAPAGE EYEWEAR BY VITALONI

K-Number: K851062 · 1985-04-01

ApplicantVitaloni S.P.A.
Decision Date1985-04-01
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DERAPAGE EYEWEAR BY VITALONI is the device name listed in this FDA 510(k) record. The listed applicant is Vitaloni S.P.A.. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K851062. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERAPAGE EYEWEAR BY VITALONI?

DERAPAGE EYEWEAR BY VITALONI is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Vitaloni S.P.A.. The 510(k) number is K851062.

When did DERAPAGE EYEWEAR BY VITALONI receive FDA 510(k) clearance?

DERAPAGE EYEWEAR BY VITALONI received FDA 510(k) clearance on 1985-04-01, under 510(k) number K851062.

Who is the listed applicant for DERAPAGE EYEWEAR BY VITALONI?

The FDA 510(k) record lists Vitaloni S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERAPAGE EYEWEAR BY VITALONI?

The FDA product code for DERAPAGE EYEWEAR BY VITALONI is HQY.

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Related Devices (Code: HQY)

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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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