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COOPER VISION I/A SYSTEM III MODEL 1500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822220
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1982
Days to Decision
72 days

COOPER VISION I/A SYSTEM III MODEL 1500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822220
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1982
Days to Decision
72 days