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FDA 510(k)

XENO MELANIN LENS

K-Number: K924548 · 1993-04-06

Decision Date1993-04-06
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

XENO MELANIN LENS is the device name listed in this FDA 510(k) record. The listed applicant is Photoprotective Technologies. It received FDA 510(k) clearance on 1993-04-06 under 510(k) number K924548. 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 XENO MELANIN LENS?

XENO MELANIN LENS is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Photoprotective Technologies. The 510(k) number is K924548.

When did XENO MELANIN LENS receive FDA 510(k) clearance?

XENO MELANIN LENS received FDA 510(k) clearance on 1993-04-06, under 510(k) number K924548.

Who is the listed applicant for XENO MELANIN LENS?

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

What is the FDA product code for XENO MELANIN LENS?

The FDA product code for XENO MELANIN LENS 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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