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DICON GLAUCOMA DIAG. CENTER 2000 SERIES

Page Type
Cleared 510(K)
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)
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