Last synced on 18 April 2025 at 11:05 pm

SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110452
510(k) Type
Special
Applicant
UNILENS CORP., USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2011
Days to Decision
63 days
Submission Type
Statement

SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110452
510(k) Type
Special
Applicant
UNILENS CORP., USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2011
Days to Decision
63 days
Submission Type
Statement