PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR
K-Number: K081865 · 2008-09-29
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Device Summary
Frequently Asked Questions
What is the PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR?
PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR is a medical device that received FDA 510(k) clearance on 2008-09-29. The listed applicant is CooperVision, Inc.. The 510(k) number is K081865.
When did PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR receive FDA 510(k) clearance?
PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR received FDA 510(k) clearance on 2008-09-29, under 510(k) number K081865.
Who is the listed applicant for PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR?
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 PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR?
The FDA product code for PROCLEAR MULTIFOCAL TORIC AND XR AND TORIC XR 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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