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CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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