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ULTRACON/ULTRACON S RIGID GAS PERMEABLE CONTACT LENS FOR DAILY WEAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980197
510(k) Type
Traditional
Applicant
SPECIALTY ULTRAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1998
Days to Decision
196 days
Submission Type
Summary

ULTRACON/ULTRACON S RIGID GAS PERMEABLE CONTACT LENS FOR DAILY WEAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980197
510(k) Type
Traditional
Applicant
SPECIALTY ULTRAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1998
Days to Decision
196 days
Submission Type
Summary