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PROCLEAR ULTRAVUE TORIC, PROCLEAR ULTRAVUE MULTIFOCAL, PROCLEAR ULTRAVUE 200T MULTIFOCAL TORIC

Page Type
Cleared 510(K)
510(k) Number
K050717
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2005
Days to Decision
53 days
Submission Type
Summary

PROCLEAR ULTRAVUE TORIC, PROCLEAR ULTRAVUE MULTIFOCAL, PROCLEAR ULTRAVUE 200T MULTIFOCAL TORIC

Page Type
Cleared 510(K)
510(k) Number
K050717
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2005
Days to Decision
53 days
Submission Type
Summary