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FDA 510(k)

RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR

K-Number: K940956 · 1994-04-11

Decision Date1994-04-11
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR is the device name listed in this FDA 510(k) record. The listed applicant is Rio Eyewear Group, Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K940956. 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 RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR?

RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Rio Eyewear Group, Inc.. The 510(k) number is K940956.

When did RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR receive FDA 510(k) clearance?

RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR received FDA 510(k) clearance on 1994-04-11, under 510(k) number K940956.

Who is the listed applicant for RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR?

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

What is the FDA product code for RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR?

The FDA product code for RIO EYEWEAR, PANAMA JACK ENVIRONMENT OPTICS, AND PARADISE RESORT EYEWEAR is HQY.

Related Clinical Trials

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.

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.

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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