FDA 510(k) Applications Submitted by ALAN J FRAZER

FDA 510(k) Number Submission Date Device Name Applicant
K110452 02/16/2011 SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2, UNILENS CORP., USA
K121652 06/05/2012 CVUE ADVANCED HYDRA VUE UNILENS CORP., USA
K082393 08/19/2008 CVUE ADVANCED (HIOXIFILCON D) SOFT (HYDROPHILIC) CONTACT LENS UNILENS CORP., USA
K142851 09/30/2014 CVue ADVANCED (hioxifilcon D) Soft (hydrophilic) Contact Lens Unilens Corp., USA


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