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FDA 510(k)

EVE COLLECTION (EYEGLASS FRAME)

K-Number: K863125 · 1986-09-03

Decision Date1986-09-03
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EVE COLLECTION (EYEGLASS FRAME) is the device name listed in this FDA 510(k) record. The listed applicant is Precision Lens Crafters. It received FDA 510(k) clearance on 1986-09-03 under 510(k) number K863125. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVE COLLECTION (EYEGLASS FRAME)?

EVE COLLECTION (EYEGLASS FRAME) is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Precision Lens Crafters. The 510(k) number is K863125.

When did EVE COLLECTION (EYEGLASS FRAME) receive FDA 510(k) clearance?

EVE COLLECTION (EYEGLASS FRAME) received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863125.

Who is the listed applicant for EVE COLLECTION (EYEGLASS FRAME)?

The FDA 510(k) record lists Precision Lens Crafters as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVE COLLECTION (EYEGLASS FRAME)?

The FDA product code for EVE COLLECTION (EYEGLASS FRAME) is HQZ.

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: HQZ)

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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