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FDA 510(k)

IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5

K-Number: K962107 · 1996-06-20

ApplicantLeonachi, Inc.
Decision Date1996-06-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5 is the device name listed in this FDA 510(k) record. The listed applicant is Leonachi, Inc.. It received FDA 510(k) clearance on 1996-06-20 under 510(k) number K962107. 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 IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5?

IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5 is a medical device that received FDA 510(k) clearance on 1996-06-20. The listed applicant is Leonachi, Inc.. The 510(k) number is K962107.

When did IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5 receive FDA 510(k) clearance?

IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5 received FDA 510(k) clearance on 1996-06-20, under 510(k) number K962107.

Who is the listed applicant for IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5?

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

What is the FDA product code for IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5?

The FDA product code for IOVES,CORTINA CLUB EYEWEAR,LOUTTESRLG5 is HQY.

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Related Devices (Code: HQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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