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INTRALASE FUSION LASER

Page Type
Cleared 510(K)
510(k) Number
K063682
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2007
Days to Decision
60 days
Submission Type
Summary

INTRALASE FUSION LASER

Page Type
Cleared 510(K)
510(k) Number
K063682
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2007
Days to Decision
60 days
Submission Type
Summary