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
K233501 10/31/2023 ôLARGAN Health AI-Techö Sleep Apnea and Sleep Quality Examination System (ST-SLP03A) Largan Medical Co., Ltd


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