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FDA 510(k) Applications Submitted by Largan Medical Co., Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K182674
09/26/2018
Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens, Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens for Astigmatism, Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens for Presbyopia
Largan Medical Co., Ltd
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