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PULSION FS LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K013941
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
90 days
Submission Type
Summary

PULSION FS LASER KERATOME

Page Type
Cleared 510(K)
510(k) Number
K013941
510(k) Type
Traditional
Applicant
INTRALASE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
90 days
Submission Type
Summary