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FDA 510(k)

SKI VECTOR NON PRECRIPTION SUNGLASSES

K-Number: K940740 · 1994-06-03

Decision Date1994-06-03
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SKI VECTOR NON PRECRIPTION SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Mountain Shades, Inc.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K940740. 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 SKI VECTOR NON PRECRIPTION SUNGLASSES?

SKI VECTOR NON PRECRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Mountain Shades, Inc.. The 510(k) number is K940740.

When did SKI VECTOR NON PRECRIPTION SUNGLASSES receive FDA 510(k) clearance?

SKI VECTOR NON PRECRIPTION SUNGLASSES received FDA 510(k) clearance on 1994-06-03, under 510(k) number K940740.

Who is the listed applicant for SKI VECTOR NON PRECRIPTION SUNGLASSES?

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

What is the FDA product code for SKI VECTOR NON PRECRIPTION SUNGLASSES?

The FDA product code for SKI VECTOR NON PRECRIPTION SUNGLASSES 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.

Other records listing Mountain Shades, Inc. as applicant

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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