BAUSCH + LOMB NESOFILCON A CONTACT LENS
K-Number: K113703 · 2012-06-05
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Device Summary
Frequently Asked Questions
What is the BAUSCH + LOMB NESOFILCON A CONTACT LENS?
BAUSCH + LOMB NESOFILCON A CONTACT LENS is a medical device that received FDA 510(k) clearance on 2012-06-05. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K113703.
When did BAUSCH + LOMB NESOFILCON A CONTACT LENS receive FDA 510(k) clearance?
BAUSCH + LOMB NESOFILCON A CONTACT LENS received FDA 510(k) clearance on 2012-06-05, under 510(k) number K113703.
Who is the listed applicant for BAUSCH + LOMB NESOFILCON A CONTACT LENS?
The FDA 510(k) record lists Bausch & Lomb, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAUSCH + LOMB NESOFILCON A CONTACT LENS?
The FDA product code for BAUSCH + LOMB NESOFILCON A 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.
Other records listing Bausch & Lomb, Incorporated as applicant
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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