COLORMAX COLOR VISION ENHANCEMENT LENSES
K-Number: K984219 · 1999-11-18
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Device Summary
Frequently Asked Questions
What is the COLORMAX COLOR VISION ENHANCEMENT LENSES?
COLORMAX COLOR VISION ENHANCEMENT LENSES is a medical device that received FDA 510(k) clearance on 1999-11-18. The listed applicant is Color Vision Technologies, Inc.. The 510(k) number is K984219.
When did COLORMAX COLOR VISION ENHANCEMENT LENSES receive FDA 510(k) clearance?
COLORMAX COLOR VISION ENHANCEMENT LENSES received FDA 510(k) clearance on 1999-11-18, under 510(k) number K984219.
Who is the listed applicant for COLORMAX COLOR VISION ENHANCEMENT LENSES?
The FDA 510(k) record lists Color Vision Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLORMAX COLOR VISION ENHANCEMENT LENSES?
The FDA product code for COLORMAX COLOR VISION ENHANCEMENT LENSES is NAI.
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.
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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