AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL
K-Number: K113245 · 2011-12-02
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Device Summary
Frequently Asked Questions
What is the AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL?
AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL is a medical device that received FDA 510(k) clearance on 2011-12-02. The listed applicant is CooperVision, Inc.. The 510(k) number is K113245.
When did AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL receive FDA 510(k) clearance?
AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL received FDA 510(k) clearance on 2011-12-02, under 510(k) number K113245.
Who is the listed applicant for AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL?
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 AVAIRA TORIC AVAIRA MULTIFOCAL?
The FDA product code for AVAIRA AVAIRA TORIC AVAIRA MULTIFOCAL 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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