Last synced on 25 January 2026 at 3:41 am

BAUSCH + LOMB BIOTURE ONEDAY FOR PRESBYOPIA (NESOFILCON A) CONTACT LENS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132715
510(k) Type
Traditional
Applicant
Bausch & Lomb Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
112 days
Submission Type
Summary

BAUSCH + LOMB BIOTURE ONEDAY FOR PRESBYOPIA (NESOFILCON A) CONTACT LENS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132715
510(k) Type
Traditional
Applicant
Bausch & Lomb Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
112 days
Submission Type
Summary