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METHAFILCON A

Page Type
Cleared 510(K)
510(k) Number
K001090
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
45 days
Submission Type
Summary

METHAFILCON A

Page Type
Cleared 510(K)
510(k) Number
K001090
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
45 days
Submission Type
Summary