Last synced on 25 January 2026 at 3:41 am

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952260
510(k) Type
Traditional
Applicant
Stellar Contact Lens, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1996
Days to Decision
233 days
Submission Type
Summary

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952260
510(k) Type
Traditional
Applicant
Stellar Contact Lens, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1996
Days to Decision
233 days
Submission Type
Summary