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DICON GLAUCOMA DIAG. CENTER 2000 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832142
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/1/1983
Days to Decision
27 days

DICON GLAUCOMA DIAG. CENTER 2000 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832142
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/1/1983
Days to Decision
27 days