AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS
K-Number: K133627 · 2013-12-23
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Device Summary
Frequently Asked Questions
What is the AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS?
AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS is a medical device that received FDA 510(k) clearance on 2013-12-23. The listed applicant is CooperVision, Inc.. The 510(k) number is K133627.
When did AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS receive FDA 510(k) clearance?
AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS received FDA 510(k) clearance on 2013-12-23, under 510(k) number K133627.
Who is the listed applicant for AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS?
The FDA product code for AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT 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 CooperVision, Inc. 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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