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CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

Page Type
Cleared 510(K)
510(k) Number
K000637
510(k) Type
Traditional
Applicant
ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/19/2000
Days to Decision
84 days
Submission Type
Statement

CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

Page Type
Cleared 510(K)
510(k) Number
K000637
510(k) Type
Traditional
Applicant
ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/19/2000
Days to Decision
84 days
Submission Type
Statement