XENO MELANIN LENS
K-Number: K924548 · 1993-04-06
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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