MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS
K-Number: K052606 · 2005-12-15
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Device Summary
Frequently Asked Questions
What is the MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS?
MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS is a medical device that received FDA 510(k) clearance on 2005-12-15. The listed applicant is Marietta Vision. The 510(k) number is K052606.
When did MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS receive FDA 510(k) clearance?
MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS received FDA 510(k) clearance on 2005-12-15, under 510(k) number K052606.
Who is the listed applicant for MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS?
The FDA 510(k) record lists Marietta Vision as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS?
The FDA product code for MARIETTA CONTACT LENS (POLYMACON), TINTED DAILY WEAR CONTACT LENS is LPL.
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: LPL)
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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