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INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3

Page Type
Cleared 510(K)
510(k) Number
K060372
510(k) Type
Traditional
Applicant
INTRA LASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2006
Days to Decision
184 days
Submission Type
Summary

INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3

Page Type
Cleared 510(K)
510(k) Number
K060372
510(k) Type
Traditional
Applicant
INTRA LASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2006
Days to Decision
184 days
Submission Type
Summary